| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:9324046-9324226 | Common:4; Rare:80 | ||||
| chr19:9538579-9538716 | Common:1; Rare:37 | ||||
| chr19:9621192-9621517 | Common:3; Rare:90 | ||||
| chr19:9675035-9675134 | Rare:27 | ||||
| chr19:9818811-9818875 | Rare:27 | ||||
| chr19:9827814-9827982 | Common:1; Rare:63 | ||||
| chr19:9834983-9835354 | Rare:146 | ||||
| chr19:10194912-10195190 | Common:1; Rare:119; Clinvar (benign):2 | ||||
| chr19:10333517-10333717 | Rare:69 | ||||
| chr19:10403417-10403929 | Rare:170 | ||||
| chr19:10565992-10566240 | Common:2; Rare:76 | ||||
| chr19:10568961-10569208 | Common:2; Rare:64 | ||||
| chr19:10928599-10928795 | Common:1; Rare:52 | ||||
| chr19:10960706-10961065 | Common:3; Rare:141 | ||||
| chr19:11089300-11089516 | Rare:37; Clinvar:9; Clinvar (pathogenic):1 |