| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:203239235-203239326 | Rare:31 | ||||
| chr2:205682356-205682567 | Rare:38 | ||||
| chr2:206085765-206085981 | Common:1; Rare:62 | ||||
| chr2:206086141-206086174 | Rare:3 | ||||
| chr2:206159380-206159989 | Common:4; Rare:182; Clinvar (benign):1 | ||||
| chr2:206765288-206765645 | Common:3; Rare:93; Clinvar:4; Clinvar (benign):4 | ||||
| chr2:207165925-207166128 | Rare:38 | ||||
| chr2:207529818-207530100 | Common:1; Rare:82 | ||||
| chr2:207625183-207625466 | Common:1; Rare:81 | ||||
| chr2:208253886-208254195 | Common:1; Rare:53 | ||||
| chr2:208254238-208254511 | Rare:70 | ||||
| chr2:208255003-208255235 | Common:2; Rare:59 | ||||
| chr2:208266070-208266348 | Common:7; Rare:93; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:210314981-210315233 | Common:7; Rare:71 | ||||
| chr2:213284200-213284508 | Rare:103 |