Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:35628894-35629099 | Common:3; Rare:58 | ||||
chr19:35745397-35745681 | Rare:87 | ||||
chr19:35757906-35758201 | Common:2; Rare:85 | ||||
chr19:35851321-35851496 | Common:1; Rare:62; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr19:35856573-35856961 | Rare:69 | ||||
chr19:35900538-35900658 | Rare:28 | ||||
chr19:36014205-36014517 | Common:2; Rare:87 | ||||
chr19:36114811-36114946 | Common:1; Rare:65 | ||||
chr19:36139834-36140087 | Rare:76 | ||||
chr19:36214633-36214736 | Rare:31 | ||||
chr19:36215058-36215179 | Rare:37 | ||||
chr19:36418616-36418690 | Rare:24 | ||||
chr19:36489511-36489653 | Common:1; Rare:32 | ||||
chr19:36528234-36528318 | Common:1; Rare:22 | ||||
chr19:36528638-36528793 | Common:3; Rare:54 |