| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:39390839-39391487 | Common:1; Rare:247 | ||||
| chr19:39406695-39406946 | Rare:101 | ||||
| chr19:39407081-39407130 | Rare:12 | ||||
| chr19:39407208-39407447 | Rare:38 | ||||
| chr19:39412308-39412648 | Common:2; Rare:135 | ||||
| chr19:39414100-39414390 | Rare:66 | ||||
| chr19:39435846-39436167 | Common:7; Rare:118 | ||||
| chr19:39445449-39445933 | Common:3; Rare:140 | ||||
| chr19:39480628-39480931 | Common:3; Rare:154; Clinvar (pathogenic):1 | ||||
| chr19:39846289-39846468 | Common:1; Rare:81 | ||||
| chr19:39970917-39971246 | Common:4; Rare:93 | ||||
| chr19:39996925-39997118 | Common:5; Rare:62 | ||||
| chr19:40056135-40056253 | Rare:16 | ||||
| chr19:40090858-40091006 | Common:1; Rare:40 | ||||
| chr19:40285193-40285441 | Common:1; Rare:80 |