| ID: 130007094 | ATAC-STARR-seq lymphoblastoid silent region 4081 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (130315951..130316010) | | |
| ID: 130007093 | ATAC-STARR-seq lymphoblastoid active region 5755 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (130315551..130315650) | | |
| ID: 130007092 | ATAC-STARR-seq lymphoblastoid active region 5754 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (130315281..130315380) | | |
| ID: 130007091 | ATAC-STARR-seq lymphoblastoid silent region 4080 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (130314211..130315040) | | |
| ID: 130007090 | ATAC-STARR-seq lymphoblastoid active region 5753 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (130314071..130314120) | | |
| ID: 127823082 | NANOG hESC enhancer GRCh37_chr11:130321509-130322010 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (130451614..130452115) | | |
| ID: 127823081 | H3K4me1 hESC enhancer GRCh37_chr11:130289647-130290148 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (130419752..130420253) | | |
| ID: 127823080 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr11:130253373-130253917 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (130383478..130384022) | | |
| ID: 127823079 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr11:130248135-130248650 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (130378240..130378755) | | |
| ID: 127823078 | NANOG hESC enhancer GRCh37_chr11:130240792-130241293 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (130370897..130371398) | | |
| ID: 126861390 | BRD4-independent group 4 enhancer GRCh37_chr11:130347582-130348781 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (130477687..130478886) | | |
| ID: 124902848 | uncharacterized LOC124902848 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (130304637..130304714, complement) | | |
| ID: 106479504 | RNA, 7SL, cytoplasmic 778, pseudogene [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (130310180..130310474) | | |
| ID: 646383 | ZBTB44 divergent transcript [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (130314993..130403657) | | |
| ID: 170689 | ADAM metallopeptidase with thrombospondin type 1 motif 15 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (130448645..130476645) | DA12 | 607509 |
| ID: 29068 | zinc finger and BTB domain containing 44 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (130226677..130314917, complement) | BTBD15, HSPC063, ZNF851 | |
| ID: 11095 | ADAM metallopeptidase with thrombospondin type 1 motif 8 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (130404923..130428609, complement) | ADAM-TS8, METH2 | 605175 |