| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:41860103-41860285 | Common:1; Rare:76; Clinvar:3; Clinvar (benign):1 | ||||
| chr19:41884142-41884469 | Rare:88 | ||||
| chr19:41898136-41898478 | Common:2; Rare:87 | ||||
| chr19:41906320-41906551 | Rare:60 | ||||
| chr19:41956873-41957120 | Rare:76 | ||||
| chr19:41959276-41959450 | Common:1; Rare:58 | ||||
| chr19:42075805-42076199 | Rare:112 | ||||
| chr19:42132409-42132629 | Rare:46 | ||||
| chr19:42217671-42217872 | Rare:78 | ||||
| chr19:42220072-42220358 | Common:2; Rare:85 | ||||
| chr19:42268368-42268593 | Rare:49 | ||||
| chr19:42302323-42302429 | Rare:39 | ||||
| chr19:42302435-42302551 | Rare:28 | ||||
| chr19:42325414-42325675 | Rare:66 | ||||
| chr19:42412411-42412644 | Common:1; Rare:39 |