| ID: 130000180 | ATAC-STARR-seq lymphoblastoid active region 27217 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (32928165..32928234) | | |
| ID: 128092250 | uncharacterized LOC128092250 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (32647202..32647390) | | |
| ID: 127459118 | OCT4-NANOG hESC enhancer GRCh37_chr8:32858695-32859305 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (33001177..33001787) | | |
| ID: 127459117 | OCT4-NANOG hESC enhancer GRCh37_chr8:32579597-32580167 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (32722079..32722649) | | |
| ID: 127459116 | OCT4-NANOG hESC enhancer GRCh37_chr8:32579026-32579596 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (32721508..32722078) | | |
| ID: 127459115 | NANOG-H3K4me1 hESC enhancer GRCh37_chr8:32504369-32504970 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (32646850..32647451) | | |
| ID: 127459114 | NANOG hESC enhancer GRCh37_chr8:32265698-32266280 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (32408182..32408764) | | |
| ID: 126860346 | BRD4-independent group 4 enhancer GRCh37_chr8:32617179-32618378 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (32759661..32760860) | | |
| ID: 126860345 | MED14-independent group 3 enhancer GRCh37_chr8:32500376-32501575 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (32642857..32644056) | | |
| ID: 126860344 | BRD4-independent group 4 enhancer GRCh37_chr8:32490269-32491468 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (32632751..32633950) | | |
| ID: 124153140 | Sharpr-MPRA regulatory region 6165 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (32323413..32323707) | | |
| ID: 114004413 | Sharpr-MPRA regulatory region 7305 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (31795313..31795607) | | |
| ID: 106481391 | RNA, U6 small nuclear 663, pseudogene [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (32911493..32911598, complement) | | |
| ID: 106479002 | RNA, 5S ribosomal pseudogene 263 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (32256496..32256623) | RN5S263 | |
| ID: 105379362 | uncharacterized LOC105379362 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (32927977..33050049) | | |
| ID: 105379361 | uncharacterized LOC105379361 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (32423620..32431649) | | |
| ID: 105379360 | uncharacterized LOC105379360 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (31535674..31542694) | | |
| ID: 100874286 | NRG1 intronic transcript 3 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (32440746..32442725) | | |
| ID: 100873516 | RNA, 5S ribosomal pseudogene 262 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (32192028..32192153, complement) | RN5S262 | |
| ID: 100873515 | RNA, 5S ribosomal pseudogene 261 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (31598099..31598204, complement) | RN5S261 | |