| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:206159384-206159982 | Common:3; Rare:180 | ||||
| chr2:206765278-206765661 | Common:3; Rare:105; Clinvar:4; Clinvar (benign):5 | ||||
| chr2:207529786-207530007 | Common:2; Rare:68 | ||||
| chr2:208255047-208255221 | Common:2; Rare:46 | ||||
| chr2:210477568-210477686 | Rare:37 | ||||
| chr2:215436004-215436234 | Common:2; Rare:73 | ||||
| chr2:216081788-216081925 | Common:1; Rare:47 | ||||
| chr2:216498740-216498894 | Common:6; Rare:65 | ||||
| chr2:218216966-218217230 | Common:2; Rare:93 | ||||
| chr2:218270106-218270538 | Common:5; Rare:131; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:218568317-218568654 | Common:3; Rare:88 | ||||
| chr2:218659606-218659757 | Rare:38 | ||||
| chr2:218671977-218672327 | Common:2; Rare:87 | ||||
| chr2:219176926-219177068 | Common:4; Rare:44 | ||||
| chr2:219229586-219229849 | Common:1; Rare:69 |