| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:98143450-98143649 | Common:1; Rare:51 | ||||
| chr4:98261152-98261529 | Common:1; Rare:121 | ||||
| chr4:98657637-98657830 | Rare:39 | ||||
| chr4:98658621-98658760 | Common:1; Rare:39 | ||||
| chr4:98929093-98929345 | Common:3; Rare:65 | ||||
| chr4:98995515-98995781 | Common:5; Rare:88 | ||||
| chr4:99088696-99088884 | Common:6; Rare:85 | ||||
| chr4:99563635-99563812 | Common:2; Rare:54 | ||||
| chr4:99563989-99564127 | Common:2; Rare:45; Clinvar:1; Clinvar (benign):2 | ||||
| chr4:99894344-99894620 | Common:3; Rare:96 | ||||
| chr4:99949727-99949945 | Common:3; Rare:82 | ||||
| chr4:99950254-99950532 | Rare:60 | ||||
| chr4:101347523-101347812 | Common:5; Rare:90 | ||||
| chr4:102760916-102761053 | Rare:46; Clinvar:1 | ||||
| chr4:102826788-102827381 | Common:5; Rare:204 |