| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:74173946-74174441 | Common:3; Rare:192 | ||||
| chr7:74254366-74254554 | Rare:89 | ||||
| chr7:74453700-74454163 | Common:1; Rare:121 | ||||
| chr7:74454484-74454489 | |||||
| chr7:74657467-74657802 | Common:2; Rare:96 | ||||
| chr7:74657959-74658067 | Common:1; Rare:21 | ||||
| chr7:75611764-75611977 | Common:1; Rare:41 | ||||
| chr7:75738918-75739310 | Common:2; Rare:108 | ||||
| chr7:75878826-75879114 | Common:12; Rare:106 | ||||
| chr7:75914911-75915189 | Common:3; Rare:101; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:75981965-75982295 | Common:2; Rare:104; Clinvar:1 | ||||
| chr7:75983287-75983563 | Common:5; Rare:77; Clinvar (pathogenic):1 | ||||
| chr7:75985429-75985734 | Common:6; Rare:118; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr7:75994493-75994781 | Common:4; Rare:141 | ||||
| chr7:76047786-76048215 | Common:3; Rare:131 |