ID: 129662299 | ReSE screen-validated silencer GRCh37_chr8:51449232-51449447 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (50536672..50536887) | | |
ID: 127459492 | OCT4-NANOG hESC enhancer GRCh37_chr8:51066297-51066804 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (50153737..50154244) | | |
ID: 127459491 | NANOG hESC enhancer GRCh37_chr8:50969100-50969624 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (50056540..50057064) | | |
ID: 127459490 | H3K4me1 hESC enhancer GRCh37_chr8:50822872-50823816 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (49910312..49911256) | | |
ID: 127459489 | H3K4me1 hESC enhancer GRCh37_chr8:50755104-50755652 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (49842544..49843092) | | |
ID: 127459488 | H3K4me1 hESC enhancer GRCh37_chr8:50754554-50755103 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (49841994..49842543) | | |
ID: 127459487 | OCT4-NANOG hESC enhancer GRCh37_chr8:50629145-50629825 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (49716585..49717265) | | |
ID: 127459486 | NANOG hESC enhancer GRCh37_chr8:50516568-50517170 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (49604009..49604611) | | |
ID: 126860383 | BRD4-independent group 4 enhancer GRCh37_chr8:50568577-50569776 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (49656017..49657216) | | |
ID: 124902098 | uncharacterized LOC124902098 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (50734258..50734366) | | |
ID: 124900619 | uncharacterized LOC124900619 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (50217891..50228749, complement) | | |
ID: 124174251 | Sharpr-MPRA regulatory region 14710 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (50662989..50663283) | | |
ID: 124174250 | Sharpr-MPRA regulatory region 15467 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (50605109..50605403) | | |
ID: 105375830 | uncharacterized LOC105375830 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (50926492..50934780, complement) | | |
ID: 105375829 | uncharacterized LOC105375829 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (50228738..50237226, complement) | | |
ID: 105375828 | uncharacterized LOC105375828 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (50364446..50376977, complement) | | |
ID: 100507464 | uncharacterized LOC100507464 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (49496763..49512180, complement) | | |
ID: 100422267 | coagulation factor III, tissue factor pseudogene [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (50490795..50491372) | | |
ID: 100128686 | programmed cell death 10 pseudogene [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (50859530..50860254) | | |
ID: 360175 | CYCS pseudogene 22 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (50762186..50762864, complement) | HCP22 | |