| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:96870308-96870389 | Rare:17 | ||||
| chr2:96870808-96870844 | Rare:8 | ||||
| chr2:97094793-97095048 | Common:1; Rare:56 | ||||
| chr2:97590273-97590560 | Common:1; Rare:56 | ||||
| chr2:97645806-97646205 | Common:3; Rare:119 | ||||
| chr2:97663886-97664247 | Common:1; Rare:117 | ||||
| chr2:98608341-98608659 | Common:1; Rare:135; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:99141147-99141246 | Common:1; Rare:34 | ||||
| chr2:99154877-99155037 | Common:1; Rare:67; Clinvar (benign):1 | ||||
| chr2:99180977-99181227 | Common:2; Rare:73 | ||||
| chr2:99337070-99337464 | Common:3; Rare:109 | ||||
| chr2:100105380-100105503 | Rare:34 | ||||
| chr2:100562639-100563064 | Common:5; Rare:127 | ||||
| chr2:100563219-100563258 | Rare:13 | ||||
| chr2:101002162-101002318 | Rare:61 |