| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:218287250-218287386 | Rare:24 | ||||
| chr2:218568300-218568598 | Common:2; Rare:83 | ||||
| chr2:218659339-218659738 | Common:4; Rare:94 | ||||
| chr2:218671967-218672339 | Common:2; Rare:93 | ||||
| chr2:219176897-219177035 | Common:3; Rare:41 | ||||
| chr2:219206683-219206923 | Rare:87 | ||||
| chr2:219229533-219229896 | Common:2; Rare:114 | ||||
| chr2:219245416-219245511 | Rare:24 | ||||
| chr2:219253869-219254056 | Common:1; Rare:58 | ||||
| chr2:219279207-219279545 | Common:3; Rare:105; Clinvar (benign):1 | ||||
| chr2:219418429-219419040 | Common:5; Rare:206; Clinvar:40; Clinvar (benign):20; Clinvar (pathogenic):3 | ||||
| chr2:219419863-219420375 | Common:4; Rare:137; Clinvar:14; Clinvar (benign):15; Clinvar (pathogenic):2 | ||||
| chr2:219420489-219420953 | Common:2; Rare:127; Clinvar:16; Clinvar (benign):16; Clinvar (pathogenic):4 | ||||
| chr2:219460587-219460867 | Common:3; Rare:61 | ||||
| chr2:219498711-219498917 | Common:2; Rare:40 |