| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:44796375-44796791 | Common:3; Rare:161 | ||||
| chr7:44999991-45000267 | Common:1; Rare:66 | ||||
| chr7:45111665-45111799 | Common:1; Rare:50 | ||||
| chr7:47979507-47979704 | Rare:81 | ||||
| chr7:48088595-48088711 | Common:1; Rare:28 | ||||
| chr7:48089039-48089245 | Common:1; Rare:51 | ||||
| chr7:50450302-50450453 | Common:1; Rare:60 | ||||
| chr7:55018918-55019240 | Common:2; Rare:90; Clinvar:1; Clinvar (benign):2 | ||||
| chr7:55365919-55366073 | Rare:67 | ||||
| chr7:55552750-55552934 | Rare:41 | ||||
| chr7:55572328-55572580 | Common:1; Rare:101 | ||||
| chr7:56051390-56051915 | Common:1; Rare:194; Clinvar:5; Clinvar (benign):1 | ||||
| chr7:56106367-56106713 | Common:9; Rare:125 | ||||
| chr7:64563063-64563252 | Common:2; Rare:47 | ||||
| chr7:64794277-64794450 | Common:3; Rare:48 |