ID: 127891861 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:47921871-47922864 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (47418614..47419607) | | |
ID: 127891860 | H3K4me1 hESC enhancer GRCh37_chr19:47920878-47921870 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (47417621..47418613) | | |
ID: 127891859 | H3K4me1 hESC enhancer GRCh37_chr19:47906547-47907244 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (47403290..47403987) | | |
ID: 127891858 | H3K4me1 hESC enhancer GRCh37_chr19:47905847-47906546 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (47402590..47403289) | | |
ID: 127891857 | H3K4me1 hESC enhancer GRCh37_chr19:47905147-47905846 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (47401890..47402589) | | |
ID: 127891856 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:47901415-47902082 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (47398158..47398825) | | |
ID: 121852990 | Sharpr-MPRA regulatory region 169 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (47429172..47429466) | | |
ID: 121627882 | hESC enhancers GRCh37_chr19:47931091-47931659 and GRCh37_chr19:47931660-47932227 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (47427834..47428970) | | |
ID: 56917 | Meis homeobox 3 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (47403124..47422233, complement) | MRG2 | 619443 |
ID: 6543 | solute carrier family 8 member A2 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (47428017..47471893, complement) | NCX2 | 601901 |