| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:218568293-218568702 | Common:4; Rare:103 | ||||
| chr2:218568767-218568942 | Common:1; Rare:51 | ||||
| chr2:218659339-218659748 | Common:4; Rare:96 | ||||
| chr2:218671966-218672348 | Common:2; Rare:96 | ||||
| chr2:218781991-218782306 | Rare:93; Clinvar:7; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr2:219160789-219160899 | Common:1; Rare:34 | ||||
| chr2:219176869-219177115 | Common:4; Rare:76 | ||||
| chr2:219206670-219206923 | Rare:91 | ||||
| chr2:219229303-219229422 | Rare:36 | ||||
| chr2:219229544-219229912 | Common:2; Rare:116 | ||||
| chr2:219245374-219245531 | Rare:46 | ||||
| chr2:219279192-219279545 | Common:3; Rare:108; Clinvar (benign):1 | ||||
| chr2:219434711-219434860 | Common:1; Rare:25 | ||||
| chr2:219441905-219442071 | Rare:37 | ||||
| chr2:219460514-219460891 | Common:3; Rare:90 |