ID: 132090835 | Neanderthal introgressed variant-containing enhancer experimental_19937 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (20465106..20465275) | | |
ID: 132089912 | Neanderthal introgressed variant-containing enhancer experimental_20020 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (20561146..20561315) | | |
ID: 132089911 | Neanderthal introgressed variant-containing enhancer experimental_19926 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (20450486..20450655) | | |
ID: 132089910 | Neanderthal introgressed variant-containing enhancer experimental_19843 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (20278548..20278717) | | |
ID: 130005436 | ATAC-STARR-seq lymphoblastoid silent region 3204 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (20489981..20490030) | | |
ID: 130005435 | ATAC-STARR-seq lymphoblastoid active region 4525 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (20360733..20360952) | | |
ID: 129662882 | ReSE screen-validated silencer GRCh37_chr11:20385467-20385609 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (20363715..20364134) | | |
ID: 129662881 | ReSE screen-validated silencer GRCh37_chr11:20234917-20235147 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (20213371..20213601) | | |
ID: 127820628 | NANOG-H3K4me1 hESC enhancer GRCh37_chr11:20566010-20566716 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (20544464..20545170) | | |
ID: 127820627 | H3K27ac hESC enhancer GRCh37_chr11:20409621-20410227 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (20388075..20388681) | | |
ID: 127820626 | H3K27ac hESC enhancer GRCh37_chr11:20409013-20409620 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (20387424..20388074) | | |
ID: 127820625 | H3K27ac hESC enhancer GRCh37_chr11:20406589-20407090 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (20384910..20385544) | | |
ID: 127820624 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr11:20364173-20364700 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (20342627..20343154) | | |
ID: 127820623 | H3K4me1 hESC enhancer GRCh37_chr11:20184527-20185028 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (20162981..20163482) | | |
ID: 127820622 | NANOG-H3K4me1 hESC enhancer GRCh37_chr11:20182903-20183402 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (20161357..20161856) | | |
ID: 127820621 | NANOG-H3K4me1 hESC enhancer GRCh37_chr11:20182401-20182902 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (20160855..20161356) | | |
ID: 126861159 | BRD4-independent group 4 enhancer GRCh37_chr11:20177816-20179015 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (20156270..20157469) | | |
ID: 124902808 | uncharacterized LOC124902808 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (20441570..20450071) | | |
ID: 111365162 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr11:20388793-20389992 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (20367247..20368446) | | |
ID: 105376584 | uncharacterized LOC105376584 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (20560068..20572998, complement) | | |