| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:190880614-190880897 | Common:4; Rare:96 | ||||
| chr2:191013966-191014357 | Common:2; Rare:122; Clinvar:2; Clinvar (benign):3 | ||||
| chr2:191020328-191020680 | Common:1; Rare:115 | ||||
| chr2:191151529-191151652 | Rare:21 | ||||
| chr2:191245257-191245487 | Common:1; Rare:74 | ||||
| chr2:191246152-191246300 | Common:1; Rare:45 | ||||
| chr2:191263238-191263354 | Rare:19 | ||||
| chr2:191677684-191677780 | Common:1; Rare:21 | ||||
| chr2:191677827-191678310 | Common:4; Rare:129 | ||||
| chr2:192194917-192195060 | Rare:27 | ||||
| chr2:195656679-195657321 | Common:2; Rare:177 | ||||
| chr2:195657546-195657690 | Rare:40 | ||||
| chr2:196068759-196068928 | Common:1; Rare:52 | ||||
| chr2:196171470-196171504 | Rare:6 | ||||
| chr2:196171515-196171883 | Common:1; Rare:119 |