ID: 129661708 | ReSE screen-validated silencer GRCh37_chr6:32013699-32013950 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (32045922..32046173) | | |
ID: 127405853 | H3K4me1 hESC enhancer GRCh37_chr6:32116858-32117395 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (32149081..32149618) | | |
ID: 127405852 | H3K4me1 hESC enhancer GRCh37_chr6:32049385-32049900 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (32081608..32082123) | | |
ID: 127405851 | H3K4me1 hESC enhancer GRCh37_chr6:32041114-32041614 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (32073337..32073837) | | |
ID: 127405850 | H3K4me1 hESC enhancer GRCh37_chr6:32040222-32041078 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (32072445..32073301) | | |
ID: 127405849 | H3K4me1 hESC enhancer GRCh37_chr6:32038327-32039327 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (32070550..32071550) | | |
ID: 127405848 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:32015753-32016386 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (32047976..32048609) | | |
ID: 127405847 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:31939702-31940412 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31971925..31972635) | | |
ID: 126859654 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr6:32014364-32015563 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (32046587..32047786) | | |
ID: 124906563 | uncharacterized LOC124906563 [Homo sapiens (human)] | | | |
ID: 124905381 | uncharacterized LOC124905381 [Homo sapiens (human)] | | | |
ID: 123620085 | Sharpr-MPRA regulatory region 2290 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (32118892..32119186) | | |
ID: 116183058 | CRISPRi-validated cis-regulatory element chr6.1802 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (32131505..32131952) | | |
ID: 110631417 | CYP21A2 5' regulatory region [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (32033425..32038438) | | |
ID: 110384692 | complement C4A (Rodgers blood group)-like [Homo sapiens (human)] | | | |
ID: 106780803 | tenascin XB recombination region [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (32041608..32046122) | | |
ID: 106780800 | CYP21A2 recombination region [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (32037872..32041144) | | |
ID: 106478999 | RNA, 5S ribosomal pseudogene 206 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (32078508..32078628, complement) | RN5S206 | |
ID: 100532746 | PPT2-EGFL8 readthrough (NMD candidate) [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (32153999..32168285) | PPT-2, PPT2 | |
ID: 100507547 | uncharacterized LOC100507547 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (32152802..32154365, complement) | | |