| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:88697789-88697909 | Common:2; Rare:38 | ||||
| chr4:89836871-89837538 | Common:5; Rare:199; Clinvar:5; Clinvar (benign):1 | ||||
| chr4:94757735-94758038 | Common:4; Rare:82 | ||||
| chr4:95549001-95549153 | Common:1; Rare:30 | ||||
| chr4:95549208-95549390 | Common:1; Rare:32 | ||||
| chr4:98261159-98261534 | Common:1; Rare:120 | ||||
| chr4:98929093-98929365 | Common:3; Rare:70 | ||||
| chr4:98995478-98995774 | Common:6; Rare:105 | ||||
| chr4:99088689-99088884 | Common:6; Rare:93 | ||||
| chr4:99321309-99321509 | Rare:49 | ||||
| chr4:99563690-99563772 | Rare:20 | ||||
| chr4:99563989-99564128 | Common:2; Rare:46; Clinvar:1; Clinvar (benign):2 | ||||
| chr4:99894362-99894600 | Common:2; Rare:88 | ||||
| chr4:99950261-99950482 | Rare:41 | ||||
| chr4:101346835-101347039 | Common:2; Rare:51 |