| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:89111371-89111621 | Common:3; Rare:94 | ||||
| chr4:89307735-89307995 | Common:2; Rare:78 | ||||
| chr4:94451731-94452002 | Common:3; Rare:88 | ||||
| chr4:98143473-98143639 | Common:1; Rare:42 | ||||
| chr4:98261132-98261432 | Common:3; Rare:99 | ||||
| chr4:98929109-98929365 | Common:3; Rare:64 | ||||
| chr4:98995397-98995816 | Common:6; Rare:145 | ||||
| chr4:99088689-99088884 | Common:6; Rare:93 | ||||
| chr4:99563981-99564158 | Common:2; Rare:52; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:99950259-99950520 | Rare:51 | ||||
| chr4:101347591-101347828 | Common:4; Rare:70 | ||||
| chr4:102760891-102761076 | Rare:62; Clinvar:1 | ||||
| chr4:102826774-102826993 | Rare:66 | ||||
| chr4:102827110-102827882 | Common:5; Rare:273 | ||||
| chr4:102827906-102828094 | Rare:59 |