| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:41331914-41332158 | Rare:54; Clinvar (benign):1 | ||||
| chr19:41352660-41352967 | Common:1; Rare:86 | ||||
| chr19:41353083-41353117 | Rare:6 | ||||
| chr19:41353212-41353267 | Rare:13; Clinvar (benign):1 | ||||
| chr19:41365873-41366024 | Common:2; Rare:26 | ||||
| chr19:41374109-41374330 | Rare:42 | ||||
| chr19:42292801-42293088 | Rare:106; Clinvar:3 | ||||
| chr19:42396905-42397184 | Common:1; Rare:66 | ||||
| chr19:43647960-43648024 | Common:1; Rare:13 | ||||
| chr19:44258462-44258584 | Rare:17 | ||||
| chr19:44321816-44322067 | Common:3; Rare:40 | ||||
| chr19:45517729-45518091 | Common:2; Rare:128 | ||||
| chr19:45859179-45859311 | Common:1; Rare:33 | ||||
| chr19:45860172-45860364 | Common:4; Rare:37 | ||||
| chr19:45883743-45883895 | Rare:19 |