ID: 132090642 | Neanderthal introgressed variant-containing enhancer experimental_63138 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (25123833..25124002) | | |
ID: 130067126 | ATAC-STARR-seq lymphoblastoid silent region 13557 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (24952533..24952782) | | |
ID: 129664828 | ReSE screen-validated silencer GRCh37_chr22:25307870-25308029 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (24911903..24912062) | | |
ID: 127895636 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:25507477-25508338 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (25111510..25112371) | | |
ID: 127895635 | H3K27ac hESC enhancer GRCh37_chr22:25506614-25507476 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (25110647..25111509) | | |
ID: 127895634 | H3K4me1 hESC enhancer GRCh37_chr22:25494863-25495382 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (25098896..25099415) | | |
ID: 127895633 | H3K4me1 hESC enhancer GRCh37_chr22:25465590-25466140 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (25069623..25070173) | | |
ID: 127895632 | H3K4me1 hESC enhancer GRCh37_chr22:25462486-25463045 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (25066519..25067078) | | |
ID: 127895631 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:25457216-25458130 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (25061249..25062163) | | |
ID: 127895630 | H3K27ac hESC enhancer GRCh37_chr22:25398411-25398910 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (25002444..25002943) | | |
ID: 127895629 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:25390751-25391348 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (24994784..24995381) | | |
ID: 127895628 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:25365545-25366128 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (24969578..24970161) | | |
ID: 127895627 | H3K27ac hESC enhancer GRCh37_chr22:25354355-25354854 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (24958388..24958887) | | |
ID: 126863102 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr22:25421915-25423114 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (25025948..25027147) | | |
ID: 125424401 | Sharpr-MPRA regulatory region 1539 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (25172202..25172496) | | |
ID: 125424400 | Sharpr-MPRA regulatory region 2564 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (25169142..25169436) | | |
ID: 125424399 | Sharpr-MPRA regulatory region 9438 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (24937202..24937496) | | |
ID: 124900481 | small nucleolar RNA SNORD56 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (24901147..24901214, complement) | | |
ID: 121627935 | Sharpr-MPRA regulatory region 10625 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (25086002..25086296) | | |
ID: 101232810 | STMN3 pseudogene 1 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (25177666..25179556, complement) | | |