| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:120066740-120066993 | Common:5; Rare:78 | ||||
| chr4:120922621-120922955 | Rare:100; Clinvar:5; Clinvar (benign):1 | ||||
| chr4:121696581-121696748 | Common:1; Rare:36 | ||||
| chr4:121696843-121697254 | Common:7; Rare:118 | ||||
| chr4:121801233-121801438 | Common:2; Rare:71 | ||||
| chr4:121823779-121824121 | Common:4; Rare:84 | ||||
| chr4:121870412-121870652 | Common:1; Rare:57; Clinvar (benign):1 | ||||
| chr4:122732383-122732824 | Common:4; Rare:143; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:122913296-122913366 | Common:2; Rare:17 | ||||
| chr4:122922510-122922666 | Common:3; Rare:80 | ||||
| chr4:122922897-122923145 | Common:2; Rare:74; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr4:123396654-123396926 | Rare:65 | ||||
| chr4:123399338-123399675 | Common:1; Rare:100 | ||||
| chr4:123400169-123400266 | Rare:23 | ||||
| chr4:124712561-124713063 | Common:1; Rare:144 |