| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:88284247-88284507 | Common:2; Rare:51 | ||||
| chr4:88284517-88284945 | Common:2; Rare:103 | ||||
| chr4:88523591-88523875 | Common:2; Rare:94 | ||||
| chr4:88592294-88592542 | Common:1; Rare:78 | ||||
| chr4:88697746-88697909 | Common:2; Rare:58 | ||||
| chr4:88737545-88737838 | Rare:58 | ||||
| chr4:88759396-88759762 | Rare:57 | ||||
| chr4:88823061-88823482 | Common:4; Rare:81 | ||||
| chr4:88823739-88823827 | Rare:21 | ||||
| chr4:89057122-89057209 | Common:1; Rare:19 | ||||
| chr4:89111077-89111174 | Rare:21 | ||||
| chr4:89111209-89111651 | Common:6; Rare:160 | ||||
| chr4:89307575-89307697 | Common:2; Rare:41 | ||||
| chr4:89307728-89307964 | Common:1; Rare:75 | ||||
| chr4:89836862-89837538 | Common:5; Rare:201; Clinvar:5; Clinvar (benign):1 |