| ID: 130000508 | ATAC-STARR-seq lymphoblastoid silent region 19244 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (64798655..64798704) | | |
| ID: 130000507 | ATAC-STARR-seq lymphoblastoid silent region 19243 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (64798535..64798644) | | |
| ID: 130000506 | ATAC-STARR-seq lymphoblastoid active region 27457 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (64756855..64757064) | | |
| ID: 130000505 | ATAC-STARR-seq lymphoblastoid active region 27456 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (64695413..64695472) | | |
| ID: 130000504 | ATAC-STARR-seq lymphoblastoid active region 27455 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (64581153..64581232) | | |
| ID: 127459658 | NANOG hESC enhancer GRCh37_chr8:65843197-65843698 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (64930962..64931463) | | |
| ID: 127459657 | NANOG hESC enhancer GRCh37_chr8:65522320-65522853 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (64609763..64610296) | | |
| ID: 127459656 | H3K4me1 hESC enhancer GRCh37_chr8:65499929-65500572 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (64587372..64588015) | | |
| ID: 127459655 | H3K4me1 hESC enhancer GRCh37_chr8:65499285-65499928 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (64586728..64587371) | | |
| ID: 124900252 | uncharacterized LOC124900252 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (64574308..64580012, complement) | | |
| ID: 105375880 | uncharacterized LOC105375880 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (65006908..65017815) | | |
| ID: 105375879 | uncharacterized LOC105375879 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (64798781..64817432) | | |
| ID: 105375878 | uncharacterized LOC105375878 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (64800599..64817603, complement) | | |
| ID: 401463 | BHLHE22 antisense RNA 1 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (64574308..64581892, complement) | | |
| ID: 27319 | basic helix-loop-helix family member e22 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (64580365..64583627) | BHLHB5, Beta3, Beta3a, CAGL85, TNRC20 | 613483 |
| ID: 9420 | cytochrome P450 family 7 subfamily B member 1 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (64586575..64798737, complement) | CBAS3, CP7B, SPG5A | 603711 |