| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:43869484-43869661 | Rare:50 | ||||
| chr7:43926373-43926463 | Rare:29 | ||||
| chr7:44044589-44044786 | Common:2; Rare:52 | ||||
| chr7:44490462-44490697 | Common:1; Rare:89 | ||||
| chr7:44573866-44574053 | Common:3; Rare:58 | ||||
| chr7:44582169-44582537 | Common:1; Rare:140 | ||||
| chr7:44606444-44606635 | Common:1; Rare:65 | ||||
| chr7:44796362-44796790 | Common:3; Rare:165 | ||||
| chr7:44999991-45000294 | Common:1; Rare:70 | ||||
| chr7:45111676-45111799 | Common:1; Rare:46 | ||||
| chr7:50450306-50450453 | Common:1; Rare:59 | ||||
| chr7:55572302-55572561 | Common:1; Rare:102 | ||||
| chr7:56051434-56051878 | Common:1; Rare:170; Clinvar:5; Clinvar (benign):1 | ||||
| chr7:66114776-66114955 | Common:1; Rare:83 | ||||
| chr7:66115194-66115354 | Rare:35 |