| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:201116212-201116429 | Rare:40 | ||||
| chr2:201118607-201118737 | Rare:27 | ||||
| chr2:201451490-201451855 | Common:2; Rare:95 | ||||
| chr2:201642629-201642764 | Rare:67 | ||||
| chr2:202265675-202265781 | Rare:40 | ||||
| chr2:202634804-202635009 | Common:4; Rare:77 | ||||
| chr2:202912138-202912298 | Common:2; Rare:54 | ||||
| chr2:203014672-203014933 | Common:1; Rare:78 | ||||
| chr2:203239240-203239310 | Rare:26 | ||||
| chr2:206085772-206085965 | Common:1; Rare:55 | ||||
| chr2:206159396-206159672 | Common:2; Rare:92 | ||||
| chr2:206765273-206765645 | Common:3; Rare:101; Clinvar:4; Clinvar (benign):4 | ||||
| chr2:208255032-208255234 | Common:2; Rare:52 | ||||
| chr2:208266032-208266302 | Common:9; Rare:97; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:213284238-213284486 | Rare:80 |