| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:38790551-38790735 | Rare:31 | ||||
| chr19:38790890-38791043 | Common:5; Rare:11 | ||||
| chr19:38831721-38832052 | Common:4; Rare:111; Clinvar (benign):1 | ||||
| chr19:38842081-38842395 | Common:2; Rare:55 | ||||
| chr19:38899523-38900039 | Rare:158 | ||||
| chr19:38930706-38930988 | Common:2; Rare:84; Clinvar:2; Clinvar (benign):3 | ||||
| chr19:39084027-39084371 | Common:1; Rare:86 | ||||
| chr19:39084900-39085039 | Common:1; Rare:24 | ||||
| chr19:39156422-39156743 | Common:3; Rare:64 | ||||
| chr19:39197099-39197264 | Rare:56 | ||||
| chr19:39385204-39385410 | Rare:43 | ||||
| chr19:39390860-39391448 | Common:1; Rare:223 | ||||
| chr19:39406699-39407056 | Rare:130 | ||||
| chr19:39407101-39407106 | Rare:1 | ||||
| chr19:39407345-39407554 | Rare:37 |