Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:37779583-37779675 | Rare:19 | ||||
chr19:38264320-38264682 | Common:5; Rare:94 | ||||
chr19:38264911-38264973 | Rare:12 | ||||
chr19:38315889-38316250 | Common:1; Rare:101 | ||||
chr19:38319843-38319901 | Rare:14 | ||||
chr19:38374698-38374953 | Common:1; Rare:104 | ||||
chr19:38618932-38619256 | Common:3; Rare:97 | ||||
chr19:38647384-38647751 | Common:3; Rare:130 | ||||
chr19:38736923-38737146 | Common:3; Rare:32 | ||||
chr19:38831762-38832070 | Common:4; Rare:92; Clinvar (benign):1 | ||||
chr19:38842209-38842469 | Rare:52 | ||||
chr19:38842681-38842795 | Rare:26 | ||||
chr19:38849877-38849972 | Common:2; Rare:56 | ||||
chr19:38899531-38900033 | Rare:154 | ||||
chr19:38930723-38930987 | Common:2; Rare:75; Clinvar:2; Clinvar (benign):3 |