| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:109815448-109815786 | Common:1; Rare:91 | ||||
| chr4:112231597-112231831 | Common:2; Rare:71 | ||||
| chr4:112636875-112637181 | Rare:83 | ||||
| chr4:112637394-112637571 | Common:3; Rare:47 | ||||
| chr4:113761091-113761357 | Common:1; Rare:65 | ||||
| chr4:113979009-113979221 | Common:3; Rare:36 | ||||
| chr4:117085511-117085575 | Common:1; Rare:17 | ||||
| chr4:118685318-118685440 | Common:2; Rare:40 | ||||
| chr4:119135729-119135982 | Common:1; Rare:38; Clinvar (benign):3 | ||||
| chr4:119212527-119212736 | Common:2; Rare:54 | ||||
| chr4:120066775-120066955 | Common:3; Rare:54 | ||||
| chr4:121696862-121697132 | Common:5; Rare:74 | ||||
| chr4:121801246-121801411 | Common:2; Rare:53 | ||||
| chr4:121823858-121824074 | Common:2; Rare:55 | ||||
| chr4:122732436-122732768 | Common:1; Rare:101; Clinvar:2; Clinvar (benign):1 |