| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:169162891-169163266 | Not yet | Common:3; Rare:74 | 223 | ||
| chr7:44986602-44986766 | Not yet | Common:2; Rare:83 | 120 | ||
| chr7:45768893-45769141 | Not yet | Common:3; Rare:71 | 159 | ||
| chr7:66493551-66493751 | Not yet | Common:3; Rare:81 | 156 | ||
| chr7:66654444-66654568 | Not yet | Rare:47 | 104 | ||
| chr7:67302394-67302742 | Not yet | Common:5; Rare:112 | 190 | ||
| chr7:73005867-73006152 | Not yet | Rare:26 | 165 | ||
| chr7:74890542-74890823 | Not yet | Common:2; Rare:86 | 167 | ||
| chr7:75358952-75359239 | Not yet | Common:1; Rare:8 | 165 | ||
| chr7:94404552-94404890 | Not yet | Rare:85; Clinvar:6; Clinvar (pathogenic):1 | 170 | ||
| chr7:94408180-94408380 | Not yet | Common:1; Rare:55; Clinvar:3 | 160 | ||
| chr7:94409317-94409804 | Not yet | Common:4; Rare:134; Clinvar:4; Clinvar (benign):8; Clinvar (pathogenic):2 | 211 | ||
| chr7:94420277-94420640 | Not yet | Rare:103; Clinvar:3; Clinvar (benign):6; Clinvar (pathogenic):1 | 189 | ||
| chr7:100335846-100336146 | Not yet | Common:1; Rare:100 | 164 | ||
| chr7:130912176-130912369 | Not yet | Common:1; Rare:31 | 155 |