| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:10836103-10836232 | Rare:60 | ||||
| chr19:10836237-10836622 | Common:3; Rare:101 | ||||
| chr19:10848351-10848455 | Rare:14 | ||||
| chr19:10870805-10871092 | Common:2; Rare:85 | ||||
| chr19:10872108-10872430 | Rare:63 | ||||
| chr19:10928580-10928894 | Common:2; Rare:105 | ||||
| chr19:10960577-10961064 | Common:8; Rare:189 | ||||
| chr19:10961190-10961332 | Rare:51 | ||||
| chr19:10961618-10961663 | Rare:8 | ||||
| chr19:11089231-11089559 | Rare:60; Clinvar:13; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr19:11090282-11090734 | Common:2; Rare:136 | ||||
| chr19:11090802-11090882 | Rare:12 | ||||
| chr19:11155668-11156167 | Common:4; Rare:138 | ||||
| chr19:11197451-11197733 | Common:1; Rare:82 | ||||
| chr19:11197783-11198029 | Common:2; Rare:71 |