| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:39385202-39385277 | Rare:10 | ||||
| chr19:39390837-39391442 | Common:1; Rare:228 | ||||
| chr19:39406586-39406926 | Common:1; Rare:105 | ||||
| chr19:39435873-39436167 | Common:6; Rare:111 | ||||
| chr19:39480710-39480945 | Common:3; Rare:119; Clinvar (pathogenic):1 | ||||
| chr19:39834091-39834242 | Rare:42 | ||||
| chr19:39846313-39846479 | Common:1; Rare:79 | ||||
| chr19:39970935-39971214 | Common:4; Rare:79 | ||||
| chr19:39996956-39997070 | Common:4; Rare:35 | ||||
| chr19:40056163-40056243 | Rare:14 | ||||
| chr19:40090878-40090969 | Common:1; Rare:25 | ||||
| chr19:40285186-40285537 | Common:1; Rare:121 | ||||
| chr19:40348364-40348739 | Common:4; Rare:123 | ||||
| chr19:40425989-40426147 | Common:1; Rare:46 | ||||
| chr19:40444253-40444518 | Common:3; Rare:83 |