Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:12736871-12737151 | Common:1; Rare:60 | ||||
chr19:12773593-12773659 | Rare:10 | ||||
chr19:12775021-12775148 | Common:2; Rare:26 | ||||
chr19:12791234-12791494 | Rare:56 | ||||
chr19:12792547-12792701 | Common:1; Rare:19 | ||||
chr19:12801778-12801957 | Common:1; Rare:63 | ||||
chr19:12838268-12838452 | Common:1; Rare:47 | ||||
chr19:12881381-12881637 | Rare:49 | ||||
chr19:12890789-12891220 | Common:2; Rare:96; Clinvar:2; Clinvar (benign):2 | ||||
chr19:12919258-12919406 | Common:1; Rare:81 | ||||
chr19:12933694-12933887 | Common:1; Rare:57 | ||||
chr19:12938270-12938590 | Common:4; Rare:106 | ||||
chr19:12938593-12938768 | Common:3; Rare:85 | ||||
chr19:12940063-12940652 | Rare:195 | ||||
chr19:12945711-12946016 | Common:2; Rare:109 |