| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:114599001-114599036 | Common:1; Rare:6 | ||||
| chr4:118685286-118685535 | Common:3; Rare:71 | ||||
| chr4:119212554-119212812 | Common:4; Rare:64 | ||||
| chr4:119538988-119539044 | Rare:11 | ||||
| chr4:119627865-119627926 | Rare:11 | ||||
| chr4:119627928-119628102 | Common:3; Rare:39 | ||||
| chr4:119628128-119628158 | Rare:4 | ||||
| chr4:119628764-119629069 | Common:8; Rare:127 | ||||
| chr4:120066754-120066977 | Common:4; Rare:67 | ||||
| chr4:120922650-120922955 | Rare:86; Clinvar:5 | ||||
| chr4:121696862-121697154 | Common:5; Rare:80 | ||||
| chr4:121801246-121801411 | Common:2; Rare:53 | ||||
| chr4:122732430-122732762 | Common:1; Rare:101; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:122922927-122923139 | Common:2; Rare:63 | ||||
| chr4:123399338-123399675 | Common:1; Rare:100 |