| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:218322986-218323310 | Common:6; Rare:109 | ||||
| chr2:218568227-218568679 | Common:6; Rare:113 | ||||
| chr2:218568733-218568929 | Common:1; Rare:52 | ||||
| chr2:218659523-218659755 | Common:1; Rare:59 | ||||
| chr2:218671977-218672348 | Common:2; Rare:92 | ||||
| chr2:218710731-218710999 | Common:2; Rare:64 | ||||
| chr2:219160780-219160983 | Common:1; Rare:58 | ||||
| chr2:219176926-219177110 | Common:4; Rare:57 | ||||
| chr2:219206681-219206923 | Rare:87 | ||||
| chr2:219229330-219229374 | Rare:13 | ||||
| chr2:219229577-219229891 | Common:2; Rare:95 | ||||
| chr2:219245417-219245531 | Rare:33 | ||||
| chr2:219279223-219279523 | Common:2; Rare:96 | ||||
| chr2:219419845-219420140 | Common:1; Rare:57; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr2:219498663-219498920 | Common:2; Rare:52 |