| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:99563936-99564173 | Common:2; Rare:78; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:99894333-99894625 | Common:3; Rare:98 | ||||
| chr4:99946545-99946775 | Rare:85 | ||||
| chr4:99950228-99950477 | Rare:55 | ||||
| chr4:101346831-101346954 | Common:1; Rare:28 | ||||
| chr4:101346958-101347239 | Common:4; Rare:77 | ||||
| chr4:101347592-101347883 | Common:4; Rare:78 | ||||
| chr4:101348036-101348194 | Rare:46 | ||||
| chr4:102501357-102501738 | Rare:110 | ||||
| chr4:102760807-102761088 | Rare:89; Clinvar:1 | ||||
| chr4:102809670-102809850 | Common:1; Rare:40 | ||||
| chr4:102825259-102825361 | Common:2; Rare:22 | ||||
| chr4:102825516-102825555 | Rare:6 | ||||
| chr4:102825742-102825818 | Rare:27 | ||||
| chr4:102826675-102826992 | Rare:89 |