Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:53789021-53789118 | Rare:20 | ||||
chr19:53832424-53832498 | Rare:17 | ||||
chr19:53834045-53834496 | Common:10; Rare:137 | ||||
chr19:53836775-53836917 | Common:5; Rare:59 | ||||
chr19:53889779-53889913 | Rare:36; Clinvar:1; Clinvar (pathogenic):2 | ||||
chr19:53959344-53959537 | Rare:32 | ||||
chr19:53960369-53960550 | Rare:34 | ||||
chr19:53961757-53961888 | Rare:26 | ||||
chr19:53961984-53962113 | Rare:36 | ||||
chr19:53979230-53979595 | Rare:59 | ||||
chr19:53980242-53980456 | Common:4; Rare:58 | ||||
chr19:54011494-54011756 | Common:3; Rare:47 | ||||
chr19:54096641-54097039 | Common:6; Rare:101 | ||||
chr19:54133861-54133925 | Common:1; Rare:1 | ||||
chr19:54136991-54137217 | Common:4; Rare:58 |