| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:7680676-7680940 | Common:4; Rare:86 | ||||
| chr19:7829882-7830241 | Common:2; Rare:99 | ||||
| chr19:7874258-7874348 | Common:1; Rare:18 | ||||
| chr19:7874360-7874518 | Common:1; Rare:41 | ||||
| chr19:7888363-7888592 | Common:2; Rare:56 | ||||
| chr19:7903453-7903970 | Common:2; Rare:174 | ||||
| chr19:7916619-7916993 | Common:1; Rare:104 | ||||
| chr19:7917485-7917641 | Rare:48 | ||||
| chr19:7917884-7917985 | Rare:22 | ||||
| chr19:7920141-7920594 | Rare:159 | ||||
| chr19:7926107-7926271 | Common:1; Rare:66 | ||||
| chr19:7929339-7929616 | Common:1; Rare:72 | ||||
| chr19:7943025-7943142 | Common:1; Rare:24 | ||||
| chr19:7943293-7943480 | Common:1; Rare:35 | ||||
| chr19:7943595-7944095 | Common:1; Rare:148; Clinvar (benign):1 |