| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:112285823-112285993 | Rare:53 | ||||
| chr4:112636860-112637187 | Common:1; Rare:91 | ||||
| chr4:112637295-112637570 | Common:3; Rare:86 | ||||
| chr4:118685318-118685440 | Common:2; Rare:40 | ||||
| chr4:119212400-119212738 | Common:3; Rare:100 | ||||
| chr4:119300711-119300848 | Common:1; Rare:51 | ||||
| chr4:119627990-119628102 | Rare:26 | ||||
| chr4:119628773-119629025 | Common:8; Rare:106 | ||||
| chr4:120066784-120066911 | Common:2; Rare:38 | ||||
| chr4:121696924-121697123 | Common:4; Rare:55 | ||||
| chr4:121801246-121801405 | Common:2; Rare:51 | ||||
| chr4:122732471-122732762 | Common:1; Rare:89; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:122922956-122923113 | Common:2; Rare:43 | ||||
| chr4:123399333-123399653 | Common:1; Rare:98 | ||||
| chr4:127632855-127632966 | Rare:26 |