| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:82900488-82900805 | Rare:101 | ||||
| chr4:83455785-83456089 | Common:2; Rare:117 | ||||
| chr4:83485084-83485287 | Common:3; Rare:85 | ||||
| chr4:85827650-85827963 | Common:1; Rare:47 | ||||
| chr4:87529059-87529466 | Common:3; Rare:67 | ||||
| chr4:88284545-88284632 | Rare:13 | ||||
| chr4:88592300-88592520 | Common:1; Rare:65 | ||||
| chr4:88823244-88823574 | Common:1; Rare:59 | ||||
| chr4:94451792-94451995 | Common:3; Rare:65 | ||||
| chr4:98261148-98261499 | Common:1; Rare:111 | ||||
| chr4:98929108-98929254 | Common:3; Rare:43 | ||||
| chr4:98995496-98995763 | Common:6; Rare:93 | ||||
| chr4:99088702-99088884 | Common:6; Rare:79 | ||||
| chr4:99563989-99564170 | Common:2; Rare:55; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:99894357-99894583 | Common:2; Rare:85 |