| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:44999582-44999743 | Common:4; Rare:60 | ||||
| chr7:45000009-45000285 | Common:1; Rare:66 | ||||
| chr7:45111664-45111799 | Common:1; Rare:51 | ||||
| chr7:48088866-48089278 | Common:6; Rare:104 | ||||
| chr7:50450309-50450453 | Common:1; Rare:59 | ||||
| chr7:55366200-55366392 | Common:1; Rare:82 | ||||
| chr7:55552752-55552908 | Rare:32 | ||||
| chr7:55572341-55572561 | Common:1; Rare:92 | ||||
| chr7:56034147-56034272 | Rare:36 | ||||
| chr7:56051404-56051854 | Common:1; Rare:171; Clinvar:5; Clinvar (benign):1 | ||||
| chr7:56106418-56106710 | Common:8; Rare:98 | ||||
| chr7:64665996-64666139 | Common:1; Rare:27 | ||||
| chr7:65006655-65006794 | Common:1; Rare:40 | ||||
| chr7:66114732-66114904 | Common:2; Rare:76 | ||||
| chr7:66115177-66115353 | Common:1; Rare:41 |