| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:100612399-100612608 | Rare:40 | ||||
| chr7:100632986-100633466 | Common:1; Rare:168; Clinvar:7; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr7:100641222-100641407 | Common:1; Rare:40 | ||||
| chr7:100641674-100642059 | Common:1; Rare:76 | ||||
| chr7:100642694-100642805 | Rare:30 | ||||
| chr7:100705842-100706186 | Common:3; Rare:123 | ||||
| chr7:100827480-100827771 | Rare:103 | ||||
| chr7:100852577-100852786 | Common:2; Rare:55 | ||||
| chr7:100867247-100867425 | Common:1; Rare:55 | ||||
| chr7:100874951-100875202 | Common:1; Rare:83 | ||||
| chr7:101085214-101085506 | Common:1; Rare:49 | ||||
| chr7:101201006-101201127 | Rare:17 | ||||
| chr7:101217850-101218216 | Common:4; Rare:119 | ||||
| chr7:101237742-101238104 | Common:4; Rare:84 | ||||
| chr7:101245000-101245172 | Common:1; Rare:73 |