| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:73683399-73683649 | Common:3; Rare:112 | ||||
| chr7:73737997-73738370 | Common:2; Rare:107 | ||||
| chr7:73738746-73739268 | Common:2; Rare:160 | ||||
| chr7:73769302-73769996 | Common:4; Rare:217 | ||||
| chr7:73769998-73770386 | Common:3; Rare:88 | ||||
| chr7:73827959-73828197 | Common:4; Rare:66 | ||||
| chr7:73828251-73828505 | Rare:43 | ||||
| chr7:73842488-73842682 | Common:6; Rare:30 | ||||
| chr7:74174104-74174423 | Common:1; Rare:159 | ||||
| chr7:74254366-74254528 | Rare:75 | ||||
| chr7:74289297-74289666 | Common:5; Rare:131 | ||||
| chr7:74453935-74454084 | Rare:42 | ||||
| chr7:74657472-74657761 | Common:2; Rare:87 | ||||
| chr7:75878847-75879111 | Common:12; Rare:99 | ||||
| chr7:75914911-75915189 | Common:3; Rare:101; Clinvar:3; Clinvar (benign):1 |