| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:112231585-112231831 | Common:2; Rare:76 | ||||
| chr4:112637022-112637187 | Common:1; Rare:50 | ||||
| chr4:112637283-112637570 | Common:3; Rare:86 | ||||
| chr4:113761075-113761109 | Rare:12 | ||||
| chr4:113761129-113761275 | Common:1; Rare:34 | ||||
| chr4:113761322-113761374 | Rare:9 | ||||
| chr4:113979582-113979708 | Common:1; Rare:30 | ||||
| chr4:118685347-118685450 | Common:2; Rare:35 | ||||
| chr4:118888748-118889030 | Common:2; Rare:79 | ||||
| chr4:119136236-119136595 | Common:2; Rare:80; Clinvar (benign):5 | ||||
| chr4:119212355-119212772 | Common:5; Rare:131 | ||||
| chr4:120066810-120066973 | Common:4; Rare:43 | ||||
| chr4:121696862-121697130 | Common:5; Rare:73 | ||||
| chr4:121801218-121801445 | Common:2; Rare:85 | ||||
| chr4:122152280-122152429 | Common:2; Rare:59 |