| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:1476596-1476757 | Rare:74 | ||||
| chr7:1504329-1504556 | Common:4; Rare:105 | ||||
| chr7:1537318-1537490 | Rare:58 | ||||
| chr7:1570018-1570176 | Common:1; Rare:49 | ||||
| chr7:1817316-1817571 | Common:1; Rare:83 | ||||
| chr7:2242161-2242312 | Common:2; Rare:79 | ||||
| chr7:2354026-2354123 | Common:1; Rare:47 | ||||
| chr7:2354835-2355332 | Common:3; Rare:213 | ||||
| chr7:2403278-2403651 | Common:1; Rare:145 | ||||
| chr7:2541421-2541581 | Common:3; Rare:58; Clinvar:2; Clinvar (benign):2 | ||||
| chr7:2555485-2555561 | Common:1; Rare:25 | ||||
| chr7:2558960-2559205 | Common:3; Rare:95 | ||||
| chr7:2762503-2762808 | Common:3; Rare:101 | ||||
| chr7:2763266-2763379 | Common:2; Rare:41 | ||||
| chr7:2764456-2764605 | Rare:36 |