ID: 129930400 | ATAC-STARR-seq lymphoblastoid silent region 802 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (43992003..43992052) | | |
ID: 129930399 | ATAC-STARR-seq lymphoblastoid silent region 801 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (43991753..43991862) | | |
ID: 129930398 | ATAC-STARR-seq lymphoblastoid active region 928 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (43970041..43970320) | | |
ID: 129930397 | ATAC-STARR-seq lymphoblastoid silent region 796 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (43946746..43946995) | | |
ID: 127268980 | H3K4me1 hESC enhancer GRCh37_chr1:44447723-44448312 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (43982051..43982640) | | |
ID: 127268979 | H3K27ac hESC enhancer GRCh37_chr1:44444767-44445358 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (43979095..43979686) | | |
ID: 127268978 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:44444176-44444766 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (43978504..43979094) | | |
ID: 127268977 | H3K4me1 hESC enhancer GRCh37_chr1:44443584-44444175 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (43977912..43978503) | | |
ID: 127268976 | H3K27ac hESC enhancer GRCh37_chr1:44440619-44441451 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (43974947..43975779) | | |
ID: 127268975 | H3K27ac hESC enhancer GRCh37_chr1:44439785-44440618 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (43974113..43974946) | | |
ID: 127268974 | H3K4me1 hESC enhancer GRCh37_chr1:44436478-44437024 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (43970806..43971352) | | |
ID: 126805726 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr1:44437355-44438554 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (43971353..43972882) | | |
ID: 126805725 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr1:44426574-44427773 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (43960902..43962101) | | |
ID: 124904167 | uncharacterized LOC124904167 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (43973365..43974865, complement) | | |
ID: 112590793 | Sharpr-MPRA regulatory region 11322 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (43994837..43995131) | | |
ID: 149473 | coiled-coil domain containing 24 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (43991599..43996528) | | |
ID: 9670 | importin 13 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (43946950..43968022) | IMP13, KAP13, LGL2, RANBP13 | 610411 |
ID: 8704 | beta-1,4-galactosyltransferase 2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (43979210..43991171) | B4Gal-T2, B4Gal-T3, beta4Gal-T2 | 604013 |
ID: 6536 | solute carrier family 6 member 9 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (43996483..44031462, complement) | GCENSG, GLYT1 | 601019 |
ID: 1802 | diphthamide biosynthesis 2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (43970010..43973369) | DEDSSH2L2, DPH2 | 603456 |