| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:42804394-42804657 | Common:2; Rare:77 | ||||
| chr3:42906040-42906189 | Common:3; Rare:42 | ||||
| chr3:43690634-43690942 | Common:4; Rare:109; Clinvar:5; Clinvar (benign):1 | ||||
| chr3:44477655-44477758 | Common:1; Rare:16 | ||||
| chr3:44729556-44729667 | Common:1; Rare:42 | ||||
| chr3:44761583-44761794 | Common:3; Rare:77 | ||||
| chr3:44861815-44861918 | Common:2; Rare:50 | ||||
| chr3:44976118-44976280 | Common:2; Rare:67 | ||||
| chr3:45146349-45146484 | Common:1; Rare:47 | ||||
| chr3:45689326-45689464 | Common:1; Rare:55 | ||||
| chr3:45995801-45995975 | Common:2; Rare:41; Clinvar:1 | ||||
| chr3:46693642-46693792 | Common:1; Rare:36 | ||||
| chr3:46979489-46979846 | Common:2; Rare:85; Clinvar:1 | ||||
| chr3:47163923-47164265 | Common:1; Rare:98 | ||||
| chr3:47380806-47381072 | Rare:84 |