| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:121696663-121696719 | Rare:8 | ||||
| chr4:121696897-121697254 | Common:6; Rare:105 | ||||
| chr4:121801018-121801418 | Common:4; Rare:119 | ||||
| chr4:121823713-121824174 | Common:4; Rare:115 | ||||
| chr4:121869918-121870029 | Rare:27 | ||||
| chr4:121870377-121870669 | Common:1; Rare:69; Clinvar (benign):1 | ||||
| chr4:122152119-122152493 | Common:2; Rare:118 | ||||
| chr4:122921990-122922080 | Rare:24 | ||||
| chr4:122922167-122922346 | Rare:62 | ||||
| chr4:122922417-122922672 | Common:3; Rare:123 | ||||
| chr4:122922921-122923199 | Common:2; Rare:83; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr4:122923359-122923486 | Common:1; Rare:22 | ||||
| chr4:123398290-123398384 | Rare:29 | ||||
| chr4:123398803-123399006 | Rare:65 | ||||
| chr4:123399274-123399567 | Common:2; Rare:89 |