ID: 129999976 | ATAC-STARR-seq lymphoblastoid silent region 18982 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22164628..22165667) | | |
ID: 129999975 | ATAC-STARR-seq lymphoblastoid silent region 18981 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22141821..22141950) | | |
ID: 129999974 | ATAC-STARR-seq lymphoblastoid silent region 18980 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22141661..22141810) | | |
ID: 128772328 | melanoma risk locus-associated MPRA allelic enhancer 8:22014424 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22156839..22156983) | | |
ID: 127458866 | H3K4me1 hESC enhancer GRCh37_chr8:22046165-22046665 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22188652..22189152) | | |
ID: 127458865 | H3K27ac hESC enhancer GRCh37_chr8:22031123-22031622 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22173610..22174109) | | |
ID: 127458864 | H3K4me1 hESC enhancer GRCh37_chr8:21997802-21998409 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22140289..22140896) | | |
ID: 127458863 | H3K4me1 hESC enhancer GRCh37_chr8:21997193-21997801 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22139680..22140288) | | |
ID: 126860323 | BRD4-independent group 4 enhancer GRCh37_chr8:22048316-22049515 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22190803..22192002) | | |
ID: 124901904 | uncharacterized LOC124901904 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22187776..22191595, complement) | | |
ID: 120766137 | HR upstream open reading frame [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22130458..22131010, complement) | HMU, MUHH, U2HR | 619257 |
ID: 203190 | leucine rich repeat LGI family member 3 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22146830..22156806, complement) | IDDMDS, LGIL4 | 608302 |
ID: 80346 | receptor accessory protein 4 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22138020..22141907, complement) | C8orf20, PP432, Yip2c | 609349 |
ID: 55806 | HR lysine demethylase and nuclear receptor corepressor [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22114419..22131052, complement) | ALUNC, AU, HSA277165, HYPT4, MUHH, MUHH1 | 602302 |
ID: 6440 | surfactant protein C [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22157383..22164479) | BRICD6, PSP-C, SFTP2, SMDP2, SP-C, SP5 | 178620 |
ID: 649 | bone morphogenetic protein 1 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22165372..22212326) | OI13, PCOLC, PCP, PCP2, TLD | 112264 |