| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:51317050-51317500 | Common:7; Rare:174 | ||||
| chr7:54759060-54759458 | Common:10; Rare:302 | ||||
| chr7:55018588-55018881 | Common:1; Rare:62 | ||||
| chr7:55018895-55019280 | Common:4; Rare:174; Clinvar:4; Clinvar (benign):4 | ||||
| chr7:55365860-55366085 | Rare:158 | ||||
| chr7:55366150-55366560 | Common:5; Rare:238 | ||||
| chr7:55572447-55572591 | Common:1; Rare:59 | ||||
| chr7:55887210-55887650 | Common:9; Rare:166 | ||||
| chr7:55951714-55951980 | Common:1; Rare:139 | ||||
| chr7:55964102-55964740 | Common:2; Rare:230 | ||||
| chr7:56033976-56034338 | Rare:170; Clinvar:1 | ||||
| chr7:56051371-56051867 | Common:2; Rare:357; Clinvar:10; Clinvar (benign):2 | ||||
| chr7:56063984-56064382 | Common:4; Rare:303 | ||||
| chr7:56106389-56106715 | Common:15; Rare:186 | ||||
| chr7:64562994-64563252 | Common:6; Rare:131 |