| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:112637319-112637570 | Common:3; Rare:77 | ||||
| chr4:112818009-112818244 | Rare:37 | ||||
| chr4:113761129-113761286 | Common:1; Rare:35 | ||||
| chr4:114598645-114598948 | Common:10; Rare:85 | ||||
| chr4:115113691-115113917 | Rare:45 | ||||
| chr4:118685318-118685450 | Common:2; Rare:42 | ||||
| chr4:118836048-118836204 | Common:1; Rare:32 | ||||
| chr4:120066421-120066448 | Rare:5 | ||||
| chr4:120066748-120066993 | Common:5; Rare:76 | ||||
| chr4:120922643-120922962 | Rare:89; Clinvar:5 | ||||
| chr4:121696862-121697105 | Common:5; Rare:68 | ||||
| chr4:121801213-121801452 | Common:2; Rare:93 | ||||
| chr4:121823786-121824121 | Common:3; Rare:83 | ||||
| chr4:121870394-121870626 | Common:1; Rare:58; Clinvar (benign):1 | ||||
| chr4:122152235-122152404 | Common:2; Rare:77 |