ID: 127891185 | H3K4me1 hESC enhancer GRCh37_chr19:33361501-33362023 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (32870595..32871117) | | |
ID: 127891184 | H3K4me1 hESC enhancer GRCh37_chr19:33360978-33361500 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (32870072..32870594) | | |
ID: 127891183 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:33358961-33359536 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (32868055..32868630) | | |
ID: 127891182 | H3K4me1 hESC enhancer GRCh37_chr19:33319941-33320462 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (32829035..32829556) | | |
ID: 106481805 | RN7SK pseudogene 22 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (32862800..32863092, complement) | | |
ID: 100421414 | GCM1 pseudogene 1 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (32823436..32824505, complement) | | |
ID: 91646 | tudor domain containing 12 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (32719767..32829580) | ECAT8 | |
ID: 11136 | solute carrier family 7 member 9 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (32830511..32869767, complement) | BAT1, CSNU3 | 604144 |