| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:118034408-118034464 | Rare:8 | ||||
| chr4:118685265-118685463 | Common:3; Rare:66 | ||||
| chr4:118888815-118889015 | Common:2; Rare:58 | ||||
| chr4:119212355-119212606 | Common:2; Rare:79 | ||||
| chr4:119212617-119212730 | Common:1; Rare:36 | ||||
| chr4:119627308-119627617 | Rare:86 | ||||
| chr4:119627990-119628382 | Common:3; Rare:67 | ||||
| chr4:119628757-119629076 | Common:8; Rare:133 | ||||
| chr4:120066769-120066988 | Common:5; Rare:64 | ||||
| chr4:120922621-120922944 | Rare:98; Clinvar:5; Clinvar (benign):1 | ||||
| chr4:121381010-121381137 | Rare:38 | ||||
| chr4:121696885-121696894 | Common:1; Rare:3 | ||||
| chr4:121696931-121697139 | Common:4; Rare:56 | ||||
| chr4:121765112-121765164 | Common:1; Rare:18 | ||||
| chr4:121801218-121801411 | Common:2; Rare:72 |