| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:202911886-202912293 | Common:2; Rare:111 | ||||
| chr2:203014636-203014925 | Common:1; Rare:89 | ||||
| chr2:203238830-203239026 | Rare:75 | ||||
| chr2:203239234-203239320 | Rare:30 | ||||
| chr2:203328071-203328432 | Common:2; Rare:132 | ||||
| chr2:203535208-203535546 | Common:3; Rare:138 | ||||
| chr2:205682356-205682502 | Rare:25 | ||||
| chr2:206085772-206085965 | Common:1; Rare:55 | ||||
| chr2:206159379-206159982 | Common:4; Rare:181; Clinvar (benign):1 | ||||
| chr2:206274916-206275041 | Rare:47 | ||||
| chr2:206765278-206765683 | Common:3; Rare:111; Clinvar:5; Clinvar (benign):6 | ||||
| chr2:207165900-207166088 | Rare:36 | ||||
| chr2:207529774-207530106 | Common:3; Rare:93 | ||||
| chr2:207625226-207625591 | Common:1; Rare:101 | ||||
| chr2:208025496-208025618 | Rare:32 |