| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:113292935-113293012 | Common:1; Rare:18 | ||||
| chr4:113761140-113761276 | Common:1; Rare:33 | ||||
| chr4:114598885-114599013 | Common:2; Rare:32 | ||||
| chr4:117085415-117085604 | Common:1; Rare:56 | ||||
| chr4:118685280-118685440 | Common:3; Rare:52 | ||||
| chr4:119212558-119212751 | Common:2; Rare:48 | ||||
| chr4:119213207-119213255 | Rare:6 | ||||
| chr4:120066764-120066973 | Common:4; Rare:57 | ||||
| chr4:121696862-121697068 | Common:5; Rare:52 | ||||
| chr4:121801218-121801411 | Common:2; Rare:72 | ||||
| chr4:122732408-122732814 | Common:3; Rare:130; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:122922897-122923157 | Common:2; Rare:77; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr4:123399338-123399653 | Common:1; Rare:96 | ||||
| chr4:127632828-127632966 | Common:1; Rare:34 | ||||
| chr4:127782072-127782398 | Common:2; Rare:93 |