| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:12791270-12791706 | Common:2; Rare:95 | ||||
| chr19:12792542-12792711 | Common:1; Rare:22 | ||||
| chr19:12801761-12802038 | Common:1; Rare:93 | ||||
| chr19:12806433-12806701 | Common:2; Rare:83; Clinvar:2; Clinvar (benign):1 | ||||
| chr19:12881359-12881676 | Rare:63 | ||||
| chr19:12881716-12881850 | Common:2; Rare:18 | ||||
| chr19:12890811-12891252 | Common:2; Rare:101; Clinvar:2; Clinvar (benign):2 | ||||
| chr19:12919317-12919476 | Common:1; Rare:80 | ||||
| chr19:12933594-12933913 | Common:1; Rare:92 | ||||
| chr19:12938057-12938733 | Common:7; Rare:229 | ||||
| chr19:12945666-12945940 | Common:2; Rare:91 | ||||
| chr19:12946201-12946365 | Rare:32 | ||||
| chr19:12956781-12956861 | Rare:20 | ||||
| chr19:12957149-12957333 | Rare:54 | ||||
| chr19:13102687-13103028 | Common:4; Rare:90 |