| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:98929093-98929397 | Common:3; Rare:76 | ||||
| chr4:98995463-98995804 | Common:6; Rare:122 | ||||
| chr4:99088697-99088900 | Common:7; Rare:91 | ||||
| chr4:99563591-99563789 | Common:2; Rare:56 | ||||
| chr4:99563989-99564123 | Common:2; Rare:43; Clinvar (benign):2 | ||||
| chr4:99894333-99894620 | Common:3; Rare:98 | ||||
| chr4:99946556-99946786 | Rare:84 | ||||
| chr4:99950205-99950510 | Common:1; Rare:76 | ||||
| chr4:101347592-101347841 | Common:4; Rare:71 | ||||
| chr4:101348056-101348132 | Rare:20 | ||||
| chr4:102760908-102761084 | Rare:62; Clinvar:1 | ||||
| chr4:102826725-102826992 | Rare:77 | ||||
| chr4:102827148-102827208 | Rare:17 | ||||
| chr4:102827248-102827346 | Common:1; Rare:34 | ||||
| chr4:102827422-102827655 | Common:1; Rare:88 |