| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:56436029-56436307 | Rare:101 | ||||
| chr4:56467542-56467694 | Common:2; Rare:64; Clinvar (benign):5 | ||||
| chr4:56656345-56656619 | Common:3; Rare:44 | ||||
| chr4:56977597-56977747 | Common:1; Rare:51 | ||||
| chr4:57109920-57110286 | Rare:123 | ||||
| chr4:65670487-65670611 | Rare:34 | ||||
| chr4:67545438-67545743 | Common:2; Rare:78 | ||||
| chr4:67701121-67701362 | Common:4; Rare:111 | ||||
| chr4:70704596-70704816 | Common:1; Rare:69 | ||||
| chr4:70902221-70902396 | Common:4; Rare:57 | ||||
| chr4:70993478-70993691 | Common:4; Rare:64 | ||||
| chr4:73258505-73258888 | Common:1; Rare:105 | ||||
| chr4:73259124-73259191 | Rare:13 | ||||
| chr4:74038687-74038924 | Rare:65 | ||||
| chr4:74099184-74099406 | Common:2; Rare:53 |