ID: 132088822 | Neanderthal introgressed variant-containing enhancer experimental_57064 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (227598359..227598528) | | |
ID: 129935739 | ATAC-STARR-seq lymphoblastoid silent region 12401 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (227593168..227593257) | | |
ID: 129935738 | ATAC-STARR-seq lymphoblastoid silent region 12400 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (227534961..227535040) | | |
ID: 129935737 | ATAC-STARR-seq lymphoblastoid silent region 12399 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (227472145..227472864) | | |
ID: 129935736 | ATAC-STARR-seq lymphoblastoid active region 17202 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (227463631..227463690) | | |
ID: 129935735 | ATAC-STARR-seq lymphoblastoid active region 17201 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (227462671..227462730) | | |
ID: 129935734 | ATAC-STARR-seq lymphoblastoid active region 17200 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (227460319..227460408) | | |
ID: 129935733 | ATAC-STARR-seq lymphoblastoid active region 17199 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (227411610..227411809) | | |
ID: 129389002 | MPRA-validated peak4069 silencer [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (227376920..227377120) | | |
ID: 127275912 | H3K4me1 hESC enhancer GRCh37_chr2:228451619-228452120 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (227586903..227587404) | | |
ID: 127275911 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:228335785-228336748 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (227471069..227472032) | | |
ID: 126806540 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr2:228235290-228236489 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (227370574..227371773) | | |
ID: 124907994 | uncharacterized LOC124907994 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (227470788..227472099, complement) | | |
ID: 124907993 | uncharacterized LOC124907993 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (227391795..227392674) | | |
ID: 117134595 | small cysteine and glycine repeat containing 9 (pseudogene) [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (227587237..227587515, complement) | KRTAP28-9, KRTAP28p1 | |
ID: 112441435 | small cysteine and glycine repeat containing 2 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (227598893..227599255) | KRTAP28-2 | |
ID: 112441428 | small cysteine and glycine repeat containing 1 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (227387683..227387949, complement) | KRTAP28-1 | |
ID: 100847081 | microRNA 5703 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (227472132..227472187) | mir-5703 | |
ID: 79853 | transmembrane 4 L six family member 20 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (227362038..227381647, complement) | PRO994, SLI5, TCCE518 | 615404 |
ID: 3267 | ArfGAP with FG repeats 1 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (227472156..227561217) | HRB, RAB, RIP | 600862 |