| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:202911617-202911716 | Rare:18 | ||||
| chr2:202911892-202912042 | Rare:31 | ||||
| chr2:202912133-202912554 | Common:4; Rare:125 | ||||
| chr2:203014626-203014886 | Common:1; Rare:75 | ||||
| chr2:203238836-203239050 | Common:1; Rare:84 | ||||
| chr2:203239220-203239320 | Rare:33 | ||||
| chr2:203328190-203328411 | Common:2; Rare:84 | ||||
| chr2:206085771-206085981 | Common:1; Rare:60 | ||||
| chr2:206159359-206160070 | Common:4; Rare:215; Clinvar (benign):1 | ||||
| chr2:206274897-206275057 | Common:1; Rare:54 | ||||
| chr2:206765310-206765670 | Common:3; Rare:93; Clinvar:5; Clinvar (benign):5 | ||||
| chr2:207529774-207530025 | Common:3; Rare:79 | ||||
| chr2:207625185-207625605 | Common:1; Rare:118 | ||||
| chr2:208025492-208025618 | Rare:34 | ||||
| chr2:208255054-208255234 | Common:2; Rare:48 |