| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:208255014-208255228 | Common:2; Rare:55 | ||||
| chr2:208266070-208266298 | Common:7; Rare:75; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:209423800-209424088 | Common:1; Rare:85 | ||||
| chr2:210002421-210002659 | Common:6; Rare:81 | ||||
| chr2:215311901-215312144 | Common:8; Rare:99 | ||||
| chr2:215435637-215435945 | Common:2; Rare:72 | ||||
| chr2:215435962-215436241 | Common:2; Rare:88 | ||||
| chr2:216081771-216081925 | Common:1; Rare:56 | ||||
| chr2:216412694-216412775 | Rare:10 | ||||
| chr2:216498740-216498886 | Common:5; Rare:60 | ||||
| chr2:218216945-218217254 | Common:2; Rare:104 | ||||
| chr2:218270104-218270532 | Common:5; Rare:130; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:218287265-218287427 | Common:1; Rare:27 | ||||
| chr2:218568307-218568698 | Common:4; Rare:97 | ||||
| chr2:218659600-218659755 | Rare:40 |