ID: 132090189 | Neanderthal introgressed variant-containing enhancer experimental_32810 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (27535571..27535740) | | |
ID: 132090188 | Neanderthal introgressed variant-containing enhancer experimental_32809 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (27525456..27525625) | | |
ID: 132090187 | Neanderthal introgressed variant-containing enhancer experimental_32807 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (27508333..27508502) | | |
ID: 132090186 | Neanderthal introgressed variant-containing enhancer experimental_32806 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (27507273..27507442) | | |
ID: 132090185 | Neanderthal introgressed variant-containing enhancer experimental_32805 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (27439526..27439695) | | |
ID: 130009445 | ATAC-STARR-seq lymphoblastoid silent region 5204 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (27621589..27622148) | | |
ID: 130009444 | ATAC-STARR-seq lymphoblastoid active region 7508 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (27483092..27483291) | | |
ID: 130009443 | ATAC-STARR-seq lymphoblastoid active region 7507 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (27455653..27455772) | | |
ID: 130009442 | ATAC-STARR-seq lymphoblastoid active region 7506 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (27450939..27450998) | | |
ID: 127825985 | H3K27ac hESC enhancer GRCh37_chr13:28194694-28195422 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (27620079..27621285) | | |
ID: 127825984 | H3K4me1 hESC enhancer GRCh37_chr13:28107645-28108145 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (27533508..27534008) | | |
ID: 127825983 | H3K4me1 hESC enhancer GRCh37_chr13:28107144-28107644 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (27533007..27533507) | | |
ID: 127825982 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr13:28023938-28024852 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (27449801..27450918) | | |
ID: 126861719 | MED14-independent group 3 enhancer GRCh37_chr13:28302713-28303912 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (27728576..27729775) | | |
ID: 126861718 | BRD4-independent group 4 enhancer GRCh37_chr13:28008622-28009821 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (27434485..27435684) | | |
ID: 124849302 | Sharpr-MPRA regulatory region 13742 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (27459412..27459706) | | |
ID: 105370129 | uncharacterized LOC105370129 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (27738704..27740135) | | |
ID: 100873768 | RNA, U6 small nuclear 63, pseudogene [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (27488138..27488232) | RNU6-63 | |
ID: 100128903 | nucleophosmin 1 pseudogene 4 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (27696073..27697302, complement) | NG4-5, NPMP4 | |
ID: 222484 | ligand of numb-protein X 2 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (27545913..27621107, complement) | PDZRN1 | 609733 |