| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:14518341-14518820 | Common:14; Rare:381 | ||||
| chr19:14529246-14529712 | Common:2; Rare:385 | ||||
| chr19:14563406-14564480 | Common:8; Rare:529; Clinvar:4; Clinvar (benign):1 | ||||
| chr19:14571947-14572109 | Common:3; Rare:103 | ||||
| chr19:14689600-14689890 | Common:3; Rare:60 | ||||
| chr19:14690019-14690128 | Common:2; Rare:46 | ||||
| chr19:15107216-15107454 | Common:2; Rare:94 | ||||
| chr19:15125128-15125332 | Rare:90 | ||||
| chr19:15125340-15125600 | Common:2; Rare:103 | ||||
| chr19:15125644-15125987 | Common:5; Rare:151 | ||||
| chr19:15272630-15273600 | Common:3; Rare:361 | ||||
| chr19:15331834-15332218 | Common:4; Rare:247 | ||||
| chr19:15332301-15332742 | Common:2; Rare:223 | ||||
| chr19:15379711-15380072 | Rare:288 | ||||
| chr19:15418951-15419298 | Common:2; Rare:122 |