| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:12791270-12791636 | Common:2; Rare:80 | ||||
| chr19:12792536-12792722 | Common:1; Rare:26 | ||||
| chr19:12801773-12802211 | Common:1; Rare:128 | ||||
| chr19:12806419-12806674 | Common:2; Rare:76; Clinvar:2; Clinvar (benign):1 | ||||
| chr19:12880922-12881078 | Rare:44 | ||||
| chr19:12881352-12881889 | Common:2; Rare:96 | ||||
| chr19:12890788-12891309 | Common:2; Rare:126; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr19:12919212-12919514 | Common:3; Rare:151 | ||||
| chr19:12933617-12933952 | Common:1; Rare:92 | ||||
| chr19:12938134-12938800 | Common:7; Rare:235 | ||||
| chr19:12945763-12945939 | Common:1; Rare:62 | ||||
| chr19:12946208-12946317 | Rare:23 | ||||
| chr19:12956774-12956890 | Rare:28 | ||||
| chr19:12956965-12957344 | Common:2; Rare:129 | ||||
| chr19:12957591-12957661 | Rare:12 |