| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:130205380-130205553 | Rare:75 | ||||
| chr7:131109866-131110136 | Common:1; Rare:50 | ||||
| chr7:131327686-131327935 | Rare:84 | ||||
| chr7:134646566-134646864 | Common:6; Rare:89 | ||||
| chr7:134779402-134779833 | Common:2; Rare:68 | ||||
| chr7:134940815-134941248 | Common:3; Rare:86 | ||||
| chr7:135148023-135148133 | Rare:30 | ||||
| chr7:135170409-135170845 | Common:3; Rare:158 | ||||
| chr7:135662357-135662579 | Common:5; Rare:112 | ||||
| chr7:136868604-136868841 | Common:1; Rare:52 | ||||
| chr7:136868970-136869312 | Common:2; Rare:68; Clinvar (benign):3 | ||||
| chr7:139036034-139036183 | Rare:35 | ||||
| chr7:139109288-139109353 | Rare:18 | ||||
| chr7:139109355-139109460 | Common:1; Rare:31 | ||||
| chr7:139341257-139341380 | Rare:29 |