ID: 132090667 | Neanderthal introgressed variant-containing enhancer experimental_419 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (160069542..160069711) | | |
ID: 129931689 | ATAC-STARR-seq lymphoblastoid silent region 1458 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (160098374..160099203) | | |
ID: 129931688 | ATAC-STARR-seq lymphoblastoid active region 1912 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (160071889..160072248) | | |
ID: 129931687 | ATAC-STARR-seq lymphoblastoid silent region 1457 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (160070122..160070351) | | |
ID: 127270612 | H3K4me1 hESC enhancer GRCh37_chr1:160085040-160085823 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (160115250..160116033) | | |
ID: 127270611 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:160083669-160084287 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (160113879..160114497) | | |
ID: 127270610 | H3K4me1 hESC enhancer GRCh37_chr1:160082429-160083048 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (160112639..160113258) | | |
ID: 127270609 | H3K4me1 hESC enhancer GRCh37_chr1:160081809-160082428 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (160112019..160112638) | | |
ID: 127270608 | H3K4me1 hESC enhancer GRCh37_chr1:160079539-160080060 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (160109749..160110270) | | |
ID: 127270607 | H3K4me1 hESC enhancer GRCh37_chr1:160070686-160071186 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (160100896..160101396) | | |
ID: 127270606 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:160067071-160067597 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (160097281..160097807) | | |
ID: 127270605 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:160066542-160067070 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (160096752..160097280) | | |
ID: 127270604 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:160066015-160066541 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (160096225..160096751) | | |
ID: 127270603 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:160054388-160054918 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (160084598..160085128) | | |
ID: 126805890 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr1:160093987-160095186 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (160124197..160125396) | | |
ID: 120893164 | Sharpr-MPRA regulatory region 2622 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (160045659..160045953) | | |
ID: 112577506 | Sharpr-MPRA regulatory region 5459 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (160108959..160109253) | | |
ID: 93185 | immunoglobulin superfamily member 8 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (160091339..160099468, complement) | CD316, CD81P3, EWI-2, EWI2, KCT-4, LIR-D1, PGRL | 606644 |
ID: 93183 | phosphatidylinositol glycan anchor biosynthesis class M [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (160024953..160031990, complement) | GPI-MT-I | 610273 |
ID: 3766 | potassium inwardly rectifying channel subfamily J member 10 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (160037467..160070160, complement) | BIRK-10, KCNJ13-PEN, KIR1.2, KIR4.1, SESAME | 602208 |