| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:56435998-56436321 | Rare:113 | ||||
| chr4:56467532-56467699 | Common:2; Rare:71; Clinvar (benign):5 | ||||
| chr4:56977574-56977785 | Common:1; Rare:81 | ||||
| chr4:57109875-57110219 | Rare:112 | ||||
| chr4:57110348-57110536 | Common:1; Rare:61 | ||||
| chr4:65670487-65670570 | Rare:23 | ||||
| chr4:67545377-67545742 | Common:2; Rare:87 | ||||
| chr4:67701105-67701382 | Common:4; Rare:130 | ||||
| chr4:67754386-67754563 | Common:2; Rare:28; Clinvar:1; Clinvar (benign):2 | ||||
| chr4:68349849-68350209 | Common:1; Rare:115 | ||||
| chr4:69860133-69860413 | Rare:54 | ||||
| chr4:70688178-70688613 | Common:2; Rare:111 | ||||
| chr4:70704675-70704808 | Common:1; Rare:40 | ||||
| chr4:70839232-70839442 | Common:2; Rare:92 | ||||
| chr4:70902164-70902413 | Common:5; Rare:91 |