| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:10122529-10122801 | Common:9; Rare:213 | ||||
| chr2:10302500-10303059 | Common:12; Rare:268 | ||||
| chr2:10448312-10448841 | Common:2; Rare:309 | ||||
| chr2:10689875-10690036 | Common:4; Rare:99 | ||||
| chr2:10812667-10813044 | Common:8; Rare:260 | ||||
| chr2:11154931-11155751 | Common:20; Rare:319 | ||||
| chr2:11344358-11344784 | Common:3; Rare:247 | ||||
| chr2:11344920-11345190 | Common:8; Rare:143 | ||||
| chr2:11465290-11465730 | Common:6; Rare:221 | ||||
| chr2:11465784-11466335 | Common:12; Rare:304 | ||||
| chr2:11746377-11746710 | Common:4; Rare:152; Clinvar:9 | ||||
| chr2:15561277-15561416 | Rare:59 | ||||
| chr2:15591342-15592089 | Common:10; Rare:336 | ||||
| chr2:17753000-17753428 | Common:11; Rare:153 | ||||
| chr2:17753733-17754169 | Common:6; Rare:215; Clinvar (benign):1 |