| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:99563989-99564122 | Common:2; Rare:42; Clinvar (benign):2 | ||||
| chr4:99894340-99894618 | Common:3; Rare:97 | ||||
| chr4:99946545-99946792 | Rare:92 | ||||
| chr4:99950205-99950527 | Common:1; Rare:83 | ||||
| chr4:101347519-101347824 | Common:5; Rare:95 | ||||
| chr4:102760924-102761067 | Rare:50; Clinvar:1 | ||||
| chr4:102825533-102825547 | Rare:2 | ||||
| chr4:102825772-102825857 | Rare:22 | ||||
| chr4:102826685-102826993 | Rare:87 | ||||
| chr4:102827105-102827425 | Common:1; Rare:118 | ||||
| chr4:102827432-102827656 | Common:1; Rare:84 | ||||
| chr4:102827675-102828299 | Common:6; Rare:198 | ||||
| chr4:102868836-102869068 | Common:2; Rare:82 | ||||
| chr4:102869226-102869361 | Rare:54 | ||||
| chr4:105708641-105708827 | Rare:59 |