| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:12610641-12611080 | Common:2; Rare:622 | ||||
| chr19:12611305-12611705 | Common:8; Rare:140 | ||||
| chr19:12640132-12640532 | Rare:163 | ||||
| chr19:12648233-12648633 | Common:1; Rare:194; Clinvar (benign):1 | ||||
| chr19:12666375-12666502 | Rare:21 | ||||
| chr19:12666568-12666971 | Rare:411; Clinvar:19 | ||||
| chr19:12668887-12669800 | Common:24; Rare:1187 | ||||
| chr19:12681006-12681633 | Common:9; Rare:764 | ||||
| chr19:12681783-12682232 | Common:17; Rare:530 | ||||
| chr19:12696340-12697150 | Common:2; Rare:604 | ||||
| chr19:12714847-12715351 | Common:14; Rare:312 | ||||
| chr19:12721177-12721944 | Rare:282 | ||||
| chr19:12722030-12722480 | Common:4; Rare:251 | ||||
| chr19:12722470-12723839 | Common:12; Rare:714 | ||||
| chr19:12723740-12724420 | Common:7; Rare:377 |