| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:206086170-206086225 | Rare:4 | ||||
| chr2:206086272-206086285 | |||||
| chr2:206159359-206159989 | Common:4; Rare:185; Clinvar (benign):1 | ||||
| chr2:206274876-206275071 | Common:1; Rare:66 | ||||
| chr2:206765273-206765668 | Common:3; Rare:110; Clinvar:4; Clinvar (benign):5 | ||||
| chr2:207529774-207530010 | Common:3; Rare:72 | ||||
| chr2:207625227-207625591 | Common:1; Rare:101 | ||||
| chr2:207711323-207711646 | Common:1; Rare:95 | ||||
| chr2:208254238-208254507 | Rare:69 | ||||
| chr2:208254944-208255234 | Common:2; Rare:71 | ||||
| chr2:208266062-208266324 | Common:8; Rare:87; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:210477560-210477707 | Rare:46 | ||||
| chr2:215311871-215312145 | Common:8; Rare:106 | ||||
| chr2:215436039-215436271 | Common:2; Rare:76 | ||||
| chr2:216081743-216081935 | Common:1; Rare:65 |