| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:102115182-102115222 | Rare:9 | ||||
| chr7:102435386-102435526 | Common:2; Rare:20 | ||||
| chr7:103311351-103312098 | Common:2; Rare:184; Clinvar (pathogenic):1 | ||||
| chr7:103316064-103316211 | Rare:38 | ||||
| chr7:103322701-103323054 | Common:2; Rare:59 | ||||
| chr7:103367547-103367983 | Rare:99 | ||||
| chr7:105013018-105013199 | Rare:66 | ||||
| chr7:105013318-105013423 | Rare:17 | ||||
| chr7:105073501-105073687 | Common:2; Rare:33 | ||||
| chr7:105078704-105078962 | Rare:50 | ||||
| chr7:105099812-105100116 | Rare:51 | ||||
| chr7:105104352-105104445 | Rare:19 | ||||
| chr7:105110175-105110479 | Rare:79 | ||||
| chr7:105115789-105115838 | Rare:10 | ||||
| chr7:105115851-105116015 | Common:4; Rare:32 |