| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:97663888-97664296 | Common:1; Rare:129 | ||||
| chr2:97713439-97713625 | Common:1; Rare:23; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:97995924-97995955 | Rare:14 | ||||
| chr2:98086999-98087199 | Common:1; Rare:53 | ||||
| chr2:98608416-98608637 | Common:1; Rare:95; Clinvar (benign):1 | ||||
| chr2:98731056-98731280 | Common:3; Rare:80 | ||||
| chr2:98869223-98869419 | Common:1; Rare:44 | ||||
| chr2:99141141-99141345 | Common:1; Rare:78 | ||||
| chr2:99141394-99141776 | Common:2; Rare:135 | ||||
| chr2:99154877-99155045 | Common:1; Rare:69; Clinvar (benign):2 | ||||
| chr2:99180891-99181226 | Common:2; Rare:108 | ||||
| chr2:99337324-99337568 | Rare:93 | ||||
| chr2:99406377-99406686 | Rare:71 | ||||
| chr2:100562660-100563059 | Common:4; Rare:123 | ||||
| chr2:101002160-101002325 | Rare:64 |