| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:11262293-11262435 | Rare:32 | ||||
| chr19:11339565-11339768 | Common:3; Rare:48 | ||||
| chr19:11346157-11346597 | Rare:96 | ||||
| chr19:11346601-11346814 | Rare:43 | ||||
| chr19:11355265-11355499 | Common:1; Rare:77 | ||||
| chr19:11374484-11374760 | Common:1; Rare:91 | ||||
| chr19:11374821-11375297 | Common:2; Rare:160 | ||||
| chr19:11380746-11381133 | Rare:109 | ||||
| chr19:11381138-11381458 | Common:2; Rare:104; Clinvar:1 | ||||
| chr19:11435104-11435288 | Common:2; Rare:47 | ||||
| chr19:11435508-11435709 | Common:3; Rare:73; Clinvar:2; Clinvar (benign):3 | ||||
| chr19:11505047-11505362 | Common:2; Rare:112 | ||||
| chr19:11505368-11505526 | Rare:62 | ||||
| chr19:11505559-11506095 | Common:2; Rare:193 | ||||
| chr19:11528766-11528936 | Common:1; Rare:38 |