| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:202238498-202238608 | Rare:37 | ||||
| chr2:202912147-202912303 | Common:1; Rare:54 | ||||
| chr2:203239215-203239310 | Rare:30 | ||||
| chr2:206085771-206085960 | Common:1; Rare:54 | ||||
| chr2:206159380-206159681 | Common:3; Rare:99; Clinvar (benign):1 | ||||
| chr2:206274504-206274710 | Rare:55 | ||||
| chr2:206274918-206275041 | Rare:45 | ||||
| chr2:206765297-206765645 | Common:3; Rare:88; Clinvar:4; Clinvar (benign):4 | ||||
| chr2:207529774-207529997 | Common:3; Rare:70 | ||||
| chr2:207625193-207625454 | Common:1; Rare:74 | ||||
| chr2:208255009-208255234 | Common:2; Rare:58 | ||||
| chr2:208266032-208266296 | Common:9; Rare:95; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:210477580-210477690 | Rare:38 | ||||
| chr2:215435637-215436086 | Common:3; Rare:107 | ||||
| chr2:215436115-215436307 | Common:1; Rare:64 |