| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:112637373-112637616 | Common:3; Rare:61 | ||||
| chr4:113293411-113293464 | Common:1; Rare:13; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:113761015-113761365 | Common:1; Rare:89 | ||||
| chr4:113979582-113979810 | Common:6; Rare:55 | ||||
| chr4:114598306-114598412 | Common:1; Rare:20 | ||||
| chr4:114598603-114599036 | Common:11; Rare:113 | ||||
| chr4:118352306-118352509 | Rare:72; Clinvar:3 | ||||
| chr4:118685339-118685552 | Common:2; Rare:61 | ||||
| chr4:119212395-119212812 | Common:4; Rare:118 | ||||
| chr4:119300497-119300928 | Common:2; Rare:190 | ||||
| chr4:119627986-119628075 | Rare:19 | ||||
| chr4:120066782-120066982 | Common:4; Rare:58 | ||||
| chr4:121696885-121697130 | Common:5; Rare:70 | ||||
| chr4:121801051-121801396 | Common:3; Rare:98 | ||||
| chr4:122152235-122152579 | Common:2; Rare:122 |