| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:35648104-35648393 | Common:1; Rare:65; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:35745397-35745695 | Rare:88 | ||||
| chr19:35748286-35748629 | Common:3; Rare:99 | ||||
| chr19:36014192-36014525 | Common:2; Rare:92 | ||||
| chr19:36054396-36054577 | Common:3; Rare:52 | ||||
| chr19:36114808-36114959 | Common:1; Rare:71 | ||||
| chr19:36214649-36214745 | Common:1; Rare:28 | ||||
| chr19:36215076-36215176 | Rare:33 | ||||
| chr19:36489506-36489633 | Common:1; Rare:27 | ||||
| chr19:36528677-36528733 | Rare:15 | ||||
| chr19:36573247-36573477 | Common:3; Rare:71 | ||||
| chr19:36666809-36666934 | Rare:37 | ||||
| chr19:36687356-36687634 | Common:3; Rare:88 | ||||
| chr19:36916019-36916358 | Common:3; Rare:57 | ||||
| chr19:37078164-37078476 | Common:3; Rare:74 |