| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:97094812-97094980 | Common:1; Rare:40 | ||||
| chr2:97589710-97590096 | Common:8; Rare:98 | ||||
| chr2:97590273-97590455 | Rare:39 | ||||
| chr2:97645843-97646186 | Common:3; Rare:103 | ||||
| chr2:97663907-97664262 | Common:1; Rare:109 | ||||
| chr2:98087016-98087167 | Rare:37 | ||||
| chr2:98346416-98346522 | Rare:33 | ||||
| chr2:98608420-98608837 | Common:2; Rare:155; Clinvar (benign):1 | ||||
| chr2:99141128-99141787 | Common:3; Rare:235 | ||||
| chr2:99154877-99155094 | Common:2; Rare:87; Clinvar (benign):3 | ||||
| chr2:99180921-99181239 | Common:2; Rare:101 | ||||
| chr2:99337329-99337464 | Rare:56 | ||||
| chr2:100322458-100322543 | Common:1; Rare:19 | ||||
| chr2:100417323-100417735 | Rare:122 | ||||
| chr2:100562665-100563309 | Common:4; Rare:214 |