| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:73005862-73006140 | Rare:29 | ||||
| chr7:74890520-74890836 | Common:3; Rare:106 | ||||
| chr7:75358962-75359306 | Common:3; Rare:18 | ||||
| chr7:75410266-75410362 | Rare:3 | ||||
| chr7:76304182-76304405 | Common:3; Rare:69; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:84509925-84510134 | Common:1; Rare:30 | ||||
| chr7:96321225-96321540 | Common:2; Rare:74 | ||||
| chr7:97972259-97972378 | Rare:29 | ||||
| chr7:99365691-99365997 | Common:1; Rare:65 | ||||
| chr7:100335870-100336146 | Common:1; Rare:90 | ||||
| chr7:100677875-100678153 | Rare:96 | ||||
| chr7:102822451-102822508 | Common:1; Rare:6 | ||||
| chr7:105013031-105013207 | Common:1; Rare:63 | ||||
| chr7:105110213-105110368 | Rare:37 | ||||
| chr7:107972994-107973189 | Rare:45; Clinvar (benign):1 |