Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:39411468-39411757 | Common:2; Rare:53 | ||||
chr19:40923997-40924262 | Common:1; Rare:55 | ||||
chr19:41500642-41500739 | Rare:15 | ||||
chr19:41531563-41531675 | Common:1; Rare:29 | ||||
chr19:42396920-42397184 | Common:1; Rare:61 | ||||
chr19:43675436-43675737 | Common:1; Rare:51 | ||||
chr19:44847587-44847651 | Rare:11 | ||||
chr19:45509348-45509523 | Common:2; Rare:50 | ||||
chr19:45717264-45717520 | Common:1; Rare:84 | ||||
chr19:46404236-46404351 | Common:1; Rare:25 | ||||
chr19:46860835-46861126 | Common:3; Rare:95 | ||||
chr19:48966255-48966729 | Rare:160; Clinvar:3; Clinvar (pathogenic):2 | ||||
chr19:49970582-49970666 | Common:1; Rare:27 | ||||
chr19:50051027-50051137 | Rare:18 | ||||
chr19:50344757-50344769 | Common:1; Rare:1 |