| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:216498740-216498894 | Common:6; Rare:65 | ||||
| chr2:218216966-218217206 | Common:2; Rare:84 | ||||
| chr2:218270062-218270574 | Common:5; Rare:164; Clinvar:5; Clinvar (benign):2 | ||||
| chr2:218292496-218292626 | Common:1; Rare:37 | ||||
| chr2:218568220-218568708 | Common:6; Rare:124 | ||||
| chr2:218568767-218568957 | Common:1; Rare:59 | ||||
| chr2:218659492-218659755 | Common:1; Rare:67 | ||||
| chr2:218671973-218672364 | Common:2; Rare:99 | ||||
| chr2:219160785-219160866 | Common:1; Rare:28 | ||||
| chr2:219176926-219177041 | Common:3; Rare:34 | ||||
| chr2:219178142-219178418 | Common:6; Rare:119 | ||||
| chr2:219206683-219206916 | Rare:86 | ||||
| chr2:219229342-219229419 | Rare:26 | ||||
| chr2:219229553-219229900 | Common:2; Rare:110 | ||||
| chr2:219245416-219245526 | Rare:30 |