| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:74174104-74174395 | Common:1; Rare:149 | ||||
| chr7:74209852-74210044 | Rare:48 | ||||
| chr7:74254366-74254528 | Rare:75 | ||||
| chr7:74453707-74454154 | Common:1; Rare:117 | ||||
| chr7:74657483-74657730 | Common:2; Rare:73 | ||||
| chr7:75486240-75486575 | Common:2; Rare:108 | ||||
| chr7:75878805-75879083 | Common:12; Rare:100 | ||||
| chr7:75914911-75915164 | Common:3; Rare:86; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:75994489-75994786 | Common:4; Rare:146 | ||||
| chr7:76047908-76048211 | Common:2; Rare:104 | ||||
| chr7:76302731-76303075 | Rare:148; Clinvar:12; Clinvar (benign):9; Clinvar (pathogenic):5 | ||||
| chr7:76303449-76303739 | Common:1; Rare:118 | ||||
| chr7:76303771-76303931 | Common:2; Rare:86; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):7 | ||||
| chr7:76510423-76510615 | Rare:43 | ||||
| chr7:76627242-76627383 | Common:5; Rare:41 |