| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:76047727-76048223 | Common:4; Rare:149 | ||||
| chr7:76302343-76303076 | Common:4; Rare:287; Clinvar:17; Clinvar (benign):13; Clinvar (pathogenic):5 | ||||
| chr7:76303824-76304010 | Common:2; Rare:94; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):5 | ||||
| chr7:76358728-76359049 | Common:1; Rare:120 | ||||
| chr7:76393161-76393310 | Common:1; Rare:47 | ||||
| chr7:76510526-76510615 | Rare:23 | ||||
| chr7:77536841-77537204 | Common:4; Rare:105 | ||||
| chr7:77537428-77537594 | Rare:62 | ||||
| chr7:77696186-77696500 | Common:1; Rare:134 | ||||
| chr7:77696926-77697168 | Common:1; Rare:97 | ||||
| chr7:77798282-77798975 | Common:1; Rare:155 | ||||
| chr7:80918975-80919391 | Common:3; Rare:139 | ||||
| chr7:82443373-82443392 | Rare:5 | ||||
| chr7:82443538-82443875 | Common:2; Rare:108 | ||||
| chr7:82443910-82444206 | Common:1; Rare:71 |