| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:37156921-37157137 | Common:1; Rare:70 | ||||
| chr2:37231557-37231712 | Common:4; Rare:86; Clinvar (benign):3 | ||||
| chr2:37324724-37324950 | Common:1; Rare:93 | ||||
| chr2:37925016-37925296 | Common:5; Rare:98 | ||||
| chr2:38076132-38076283 | Rare:38 | ||||
| chr2:38602877-38603183 | Common:4; Rare:122 | ||||
| chr2:38751339-38751616 | Common:3; Rare:128 | ||||
| chr2:38875902-38876062 | Common:1; Rare:55 | ||||
| chr2:39437078-39437453 | Common:4; Rare:134 | ||||
| chr2:43595992-43596205 | Common:1; Rare:73 | ||||
| chr2:43637094-43637342 | Common:2; Rare:82 | ||||
| chr2:44361767-44361986 | Common:1; Rare:65 | ||||
| chr2:46297204-46297419 | Common:3; Rare:77 | ||||
| chr2:46616999-46617262 | Common:7; Rare:116 | ||||
| chr2:46699080-46699367 | Common:1; Rare:87 |