| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:44796388-44796769 | Common:3; Rare:151 | ||||
| chr7:45111655-45111816 | Common:1; Rare:64 | ||||
| chr7:45157540-45157838 | Common:2; Rare:82 | ||||
| chr7:47979507-47979757 | Rare:93 | ||||
| chr7:50450322-50450473 | Common:1; Rare:73 | ||||
| chr7:55572320-55572591 | Common:1; Rare:105 | ||||
| chr7:56051550-56051851 | Rare:129; Clinvar:4 | ||||
| chr7:56106413-56106671 | Common:7; Rare:93 | ||||
| chr7:56116364-56116468 | Rare:20 | ||||
| chr7:64307243-64307426 | Common:2; Rare:46 | ||||
| chr7:64562983-64563261 | Common:5; Rare:81 | ||||
| chr7:66075690-66075963 | Rare:64; Clinvar (benign):1 | ||||
| chr7:66114792-66114963 | Common:1; Rare:76 | ||||
| chr7:66115186-66115353 | Rare:38 | ||||
| chr7:66682028-66682192 | Common:6; Rare:77 |