| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:40285226-40285558 | Common:1; Rare:116 | ||||
| chr19:40341933-40342046 | Rare:27 | ||||
| chr19:40348331-40348739 | Common:4; Rare:132 | ||||
| chr19:40425990-40426148 | Common:1; Rare:46 | ||||
| chr19:40576737-40576900 | Common:3; Rare:50 | ||||
| chr19:40750673-40750922 | Common:1; Rare:46 | ||||
| chr19:40751049-40751332 | Common:3; Rare:83 | ||||
| chr19:40777909-40778301 | Common:1; Rare:107 | ||||
| chr19:41262387-41262566 | Rare:31 | ||||
| chr19:41264985-41265143 | Common:1; Rare:35 | ||||
| chr19:41364147-41364345 | Rare:58 | ||||
| chr19:41860107-41860518 | Common:5; Rare:158; Clinvar:4; Clinvar (benign):2 | ||||
| chr19:41959292-41959439 | Common:1; Rare:51 | ||||
| chr19:42075773-42076199 | Common:5; Rare:125 | ||||
| chr19:42220128-42220377 | Common:2; Rare:65 |