ID: 127890573 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:13319630-13320530 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (13208816..13209716) | | |
ID: 127890572 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:13297985-13298895 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (13187171..13188081) | | |
ID: 127882573 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:13297074-13297984 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (13186260..13187170) | | |
ID: 117125598 | CRISPRi-FlowFISH-validated PRDX2 regulatory element 7 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (13191111..13191611) | | |
ID: 112543458 | Sharpr-MPRA regulatory region 13602 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (13185975..13186269) | | |
ID: 108663985 | calcium voltage-gated channel subunit alpha1 A repeat instability region [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (13207859..13207898) | | |
ID: 773 | calcium voltage-gated channel subunit alpha1 A [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (13206442..13506479, complement) | APCA, BI, CACNL1A4, CAV2.1, DEE42, EA2, EIEE42, FHM, HPCA, MHP, MHP1, SCA6 | 601011 |