| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:203014626-203014933 | Common:1; Rare:98 | ||||
| chr2:203238768-203239030 | Common:1; Rare:91 | ||||
| chr2:203239240-203239251 | Rare:6 | ||||
| chr2:203328084-203328453 | Common:2; Rare:134 | ||||
| chr2:205682207-205682642 | Rare:97 | ||||
| chr2:206085824-206085969 | Common:1; Rare:39 | ||||
| chr2:206159362-206160057 | Common:4; Rare:210; Clinvar (benign):1 | ||||
| chr2:206274504-206274765 | Common:1; Rare:76 | ||||
| chr2:206274921-206275041 | Rare:44 | ||||
| chr2:206765284-206765654 | Common:3; Rare:103; Clinvar:4; Clinvar (benign):5 | ||||
| chr2:207165800-207166088 | Rare:54 | ||||
| chr2:207529748-207530108 | Common:3; Rare:105 | ||||
| chr2:208025499-208025618 | Rare:30 | ||||
| chr2:208255019-208255235 | Common:2; Rare:56 | ||||
| chr2:208266070-208266341 | Common:7; Rare:90; Clinvar:1; Clinvar (benign):2 |