| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:98658589-98658938 | Common:2; Rare:101 | ||||
| chr4:98929101-98929366 | Common:3; Rare:66 | ||||
| chr4:98995491-98995774 | Common:6; Rare:100 | ||||
| chr4:99088696-99088884 | Common:6; Rare:85 | ||||
| chr4:99946557-99946759 | Rare:71 | ||||
| chr4:99950248-99950527 | Rare:60 | ||||
| chr4:101347527-101347830 | Common:5; Rare:94 | ||||
| chr4:102826668-102826985 | Rare:84 | ||||
| chr4:102827041-102827409 | Common:4; Rare:136 | ||||
| chr4:102827439-102828094 | Common:4; Rare:214 | ||||
| chr4:102868873-102869057 | Common:2; Rare:58 | ||||
| chr4:105708637-105708827 | Rare:61 | ||||
| chr4:106316154-106316604 | Common:5; Rare:145 | ||||
| chr4:107824485-107824735 | Common:1; Rare:52 | ||||
| chr4:107989690-107989927 | Common:5; Rare:109; Clinvar:4; Clinvar (benign):5 |