| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:57709161-57709279 | Common:2; Rare:44 | ||||
| chr19:57888968-57889202 | Common:1; Rare:78 | ||||
| chr19:58059164-58059279 | Rare:60 | ||||
| chr19:58098208-58098474 | Common:8; Rare:101 | ||||
| chr19:58183315-58183429 | Rare:40 | ||||
| chr19:58278740-58279010 | Common:3; Rare:85 | ||||
| chr19:58326875-58327043 | Common:1; Rare:38 | ||||
| chr19:58347522-58347762 | Common:7; Rare:106 | ||||
| chr19:58499212-58499545 | Common:2; Rare:108; Clinvar:4; Clinvar (benign):1 | ||||
| chr19:58554939-58555210 | Common:2; Rare:86 | ||||
| chr19:58573511-58573725 | Common:4; Rare:55 | ||||
| chr2:264005-264137 | Common:2; Rare:45 | ||||
| chr2:264552-264964 | Common:4; Rare:149 | ||||
| chr2:677376-677518 | Common:1; Rare:53 | ||||
| chr2:3519492-3519645 | Common:2; Rare:48 |