| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49580536-49580650 | Rare:38 | ||||
| chr19:49640092-49640597 | Common:1; Rare:145 | ||||
| chr19:49665784-49666004 | Common:2; Rare:114; Clinvar (pathogenic):1 | ||||
| chr19:49867543-49867643 | Common:2; Rare:34 | ||||
| chr19:49877304-49877560 | Rare:59 | ||||
| chr19:49877867-49878161 | Common:3; Rare:94 | ||||
| chr19:49928620-49928978 | Common:3; Rare:81 | ||||
| chr19:49929007-49929211 | Common:3; Rare:65 | ||||
| chr19:50511084-50511580 | Common:4; Rare:159 | ||||
| chr19:51124798-51125169 | Rare:118 | ||||
| chr19:51142221-51142537 | Common:1; Rare:85 | ||||
| chr19:51366282-51366552 | Common:5; Rare:83; Clinvar (benign):2 | ||||
| chr19:51751793-51752098 | Common:2; Rare:66 | ||||
| chr19:51752275-51752417 | Rare:32 | ||||
| chr19:52008173-52008508 | Common:2; Rare:76 |