Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:23274207-23274351 | Common:1; Rare:34 | ||||
chr19:27793370-27793477 | Common:1; Rare:28 | ||||
chr19:27793669-27794024 | Rare:93 | ||||
chr19:36797291-36797559 | Common:1; Rare:59 | ||||
chr19:41352887-41352967 | Rare:22 | ||||
chr19:41353030-41353090 | Common:1; Rare:21 | ||||
chr19:41500583-41500740 | Rare:26 | ||||
chr19:41531561-41531708 | Common:1; Rare:35 | ||||
chr19:42270469-42270607 | Rare:18 | ||||
chr19:42287110-42287425 | Common:1; Rare:103; Clinvar:2 | ||||
chr19:42396922-42397184 | Common:1; Rare:61 | ||||
chr19:46133315-46133585 | Rare:47 | ||||
chr19:46860781-46861111 | Common:3; Rare:107 | ||||
chr19:48873043-48873321 | Common:2; Rare:55 | ||||
chr19:48966277-48966705 | Rare:143; Clinvar:1; Clinvar (pathogenic):2 |