| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:201642641-201642736 | Rare:49 | ||||
| chr2:206159396-206159672 | Common:2; Rare:92 | ||||
| chr2:206765293-206765604 | Common:1; Rare:75; Clinvar:3 | ||||
| chr2:208255066-208255232 | Common:2; Rare:45 | ||||
| chr2:218270202-218270532 | Common:3; Rare:91; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:218659370-218659733 | Common:3; Rare:84 | ||||
| chr2:219206690-219206880 | Rare:76 | ||||
| chr2:219245401-219245520 | Rare:30 | ||||
| chr2:232550566-232550716 | Rare:56 | ||||
| chr2:233854509-233854720 | Common:4; Rare:54 | ||||
| chr2:237085614-237085959 | Common:4; Rare:107 | ||||
| chr2:237487076-237487277 | Common:3; Rare:50 | ||||
| chr2:241315150-241315277 | Rare:49 | ||||
| chr2:241315656-241315956 | Common:4; Rare:118 | ||||
| chr20:2652480-2652644 | Common:5; Rare:49 |