| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:40750545-40750909 | Common:3; Rare:80 | ||||
| chr19:40751033-40751259 | Common:1; Rare:67 | ||||
| chr19:40777934-40778280 | Common:1; Rare:97 | ||||
| chr19:40798769-40799242 | Common:6; Rare:170 | ||||
| chr19:41218697-41218992 | Common:8; Rare:62 | ||||
| chr19:41219100-41219257 | Rare:27 | ||||
| chr19:41262336-41262566 | Rare:44 | ||||
| chr19:41310133-41310299 | Rare:72 | ||||
| chr19:41363893-41364014 | Rare:46; Clinvar:1 | ||||
| chr19:41397332-41397606 | Common:4; Rare:71 | ||||
| chr19:41860125-41860285 | Common:1; Rare:63; Clinvar:3; Clinvar (benign):1 | ||||
| chr19:41959288-41959468 | Common:1; Rare:58 | ||||
| chr19:41992956-41993326 | Rare:53 | ||||
| chr19:42075805-42076199 | Rare:112 | ||||
| chr19:42132416-42132611 | Rare:41 |