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: 127891181 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:33308781-33309375 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (32817875..32818469) | | |
ID: 127891180 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:33308187-33308780 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (32817281..32817874) | | |
ID: 127891179 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:33307591-33308186 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (32816685..32817280) | | |
ID: 127891178 | H3K4me1 hESC enhancer GRCh37_chr19:33303165-33303664 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (32812250..32812758) | | |
ID: 127891177 | H3K4me1 hESC enhancer GRCh37_chr19:33302663-33303164 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (32811757..32812258) | | |
ID: 127891176 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:33270291-33271101 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (32779385..32780195) | | |
ID: 126862893 | BRD4-independent group 4 enhancer GRCh37_chr19:33190064-33191263 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (32699158..32700357) | | |
ID: 124904690 | uncharacterized LOC124904690 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (32692965..32700147, complement) | | |
ID: 121852986 | Sharpr-MPRA regulatory region 1108 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (32787523..32787817) | | |
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: 390916 | nudix hydrolase 19 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (32691821..32713792) | RP2 | |
ID: 388531 | regulator of G protein signaling 9 binding protein [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (32675848..32678300) | PERRS, PERRS2, R9AP, RGS9 | 607814 |
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 |