| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:113214413-113214447 | Common:2; Rare:3 | ||||
| chr4:113980380-113980636 | Rare:47 | ||||
| chr4:118279109-118279190 | Common:3; Rare:20 | ||||
| chr4:118591683-118591818 | Rare:54 | ||||
| chr4:119454590-119454904 | Common:15; Rare:105 | ||||
| chr4:121449499-121449853 | Common:4; Rare:58 | ||||
| chr4:125314785-125315199 | Common:4; Rare:108 | ||||
| chr4:125315716-125315879 | Common:2; Rare:32 | ||||
| chr4:134627506-134627627 | Rare:26 | ||||
| chr4:139177890-139178159 | Rare:85 | ||||
| chr4:139387778-139388011 | Common:1; Rare:53 | ||||
| chr4:140756843-140756883 | Rare:11 | ||||
| chr4:140756994-140757183 | Rare:35 | ||||
| chr4:141332612-141332936 | Common:1; Rare:78 | ||||
| chr4:168890802-168891009 | Common:1; Rare:53; Clinvar:3; Clinvar (benign):1 |