| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:90127266-90127599 | Common:1; Rare:110 | ||||
| chr4:94451792-94451995 | Common:3; Rare:65 | ||||
| chr4:95548796-95549571 | Common:5; Rare:210 | ||||
| chr4:98143214-98143295 | Common:1; Rare:16 | ||||
| chr4:98143454-98143649 | Common:1; Rare:48 | ||||
| chr4:98261194-98261550 | Common:1; Rare:120 | ||||
| chr4:98658605-98658919 | Common:2; Rare:88 | ||||
| chr4:98929015-98929398 | Common:3; Rare:108 | ||||
| chr4:98995491-98995781 | Common:6; Rare:102 | ||||
| chr4:99088689-99088894 | Common:7; Rare:99 | ||||
| chr4:99144278-99144539 | Common:3; Rare:37 | ||||
| chr4:99321311-99321513 | Rare:48 | ||||
| chr4:99352729-99353153 | Common:2; Rare:95 | ||||
| chr4:99563593-99563785 | Common:2; Rare:54 | ||||
| chr4:99563924-99564141 | Common:2; Rare:76; Clinvar:2; Clinvar (benign):2 |