| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:39480716-39480931 | Common:3; Rare:114; Clinvar (pathogenic):1 | ||||
| chr19:39846296-39846468 | Common:1; Rare:79 | ||||
| chr19:39970918-39971214 | Common:4; Rare:82 | ||||
| chr19:39996924-39997101 | Common:5; Rare:57 | ||||
| chr19:40056163-40056262 | Rare:15 | ||||
| chr19:40090865-40091006 | Common:1; Rare:38 | ||||
| chr19:40285167-40285537 | Common:1; Rare:124 | ||||
| chr19:40348388-40348739 | Common:4; Rare:117 | ||||
| chr19:40366136-40366507 | Rare:76 | ||||
| chr19:40369953-40370237 | Rare:95 | ||||
| chr19:40376388-40376770 | Common:2; Rare:101 | ||||
| chr19:40377783-40377998 | Common:1; Rare:84 | ||||
| chr19:40444222-40444518 | Common:3; Rare:97 | ||||
| chr19:40465678-40466143 | Common:4; Rare:145 | ||||
| chr19:40580479-40580645 | Rare:59 |