| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:86594040-86594353 | Rare:100 | ||||
| chr4:87006876-87007227 | Common:4; Rare:92 | ||||
| chr4:88523698-88523856 | Common:2; Rare:55 | ||||
| chr4:89057125-89057256 | Common:1; Rare:29 | ||||
| chr4:89111223-89111635 | Common:5; Rare:152 | ||||
| chr4:89837122-89837504 | Common:3; Rare:120; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:94207839-94207931 | Rare:37 | ||||
| chr4:94451750-94451987 | Common:3; Rare:80 | ||||
| chr4:98143468-98143642 | Common:1; Rare:42 | ||||
| chr4:98261136-98261493 | Common:1; Rare:117 | ||||
| chr4:98929093-98929365 | Common:3; Rare:70 | ||||
| chr4:98995505-98995756 | Common:5; Rare:89 | ||||
| chr4:99088704-99088891 | Common:6; Rare:82 | ||||
| chr4:99563601-99563781 | Common:2; Rare:48 | ||||
| chr4:99563989-99564170 | Common:2; Rare:55; Clinvar:2; Clinvar (benign):2 |