| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:30594732-30595113 | Common:6; Rare:176; Clinvar:9; Clinvar (benign):14 | ||||
| chr7:32490354-32490507 | Common:1; Rare:47 | ||||
| chr7:32495249-32495583 | Rare:86 | ||||
| chr7:33062707-33062911 | Common:3; Rare:87 | ||||
| chr7:33129232-33129571 | Common:5; Rare:95 | ||||
| chr7:35800936-35801262 | Common:2; Rare:138 | ||||
| chr7:36389611-36389890 | Common:3; Rare:95 | ||||
| chr7:39566268-39566458 | Common:1; Rare:90 | ||||
| chr7:39623460-39623822 | Rare:115 | ||||
| chr7:40134581-40135023 | Rare:138; Clinvar:1 | ||||
| chr7:42932139-42932424 | Rare:118 | ||||
| chr7:43650001-43650021 | Rare:3 | ||||
| chr7:43729453-43729597 | Common:1; Rare:43 | ||||
| chr7:43758522-43758733 | Common:1; Rare:48 | ||||
| chr7:43869458-43869663 | Rare:66 |