| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:10286903-10286955 | Rare:11 | ||||
| chr19:10315913-10316052 | Common:4; Rare:75; Clinvar (benign):8 | ||||
| chr19:10333422-10333799 | Common:1; Rare:128 | ||||
| chr19:10339570-10339861 | Common:1; Rare:73 | ||||
| chr19:10339863-10340100 | Common:1; Rare:32 | ||||
| chr19:10380396-10381037 | Common:14; Rare:181; Clinvar:5 | ||||
| chr19:10403420-10403733 | Rare:124 | ||||
| chr19:10416561-10416608 | Common:1; Rare:5 | ||||
| chr19:10419517-10419760 | Rare:55 | ||||
| chr19:10420177-10420559 | Common:1; Rare:101 | ||||
| chr19:10430629-10430904 | Common:2; Rare:64 | ||||
| chr19:10432015-10432363 | Common:4; Rare:93 | ||||
| chr19:10502218-10502511 | Common:1; Rare:61 | ||||
| chr19:10502615-10503067 | Common:1; Rare:122 | ||||
| chr19:10503268-10503446 | Rare:39 |