| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:218125884-218126115 | Rare:41 | ||||
| chr2:218217023-218217299 | Common:2; Rare:90 | ||||
| chr2:218270107-218270485 | Common:5; Rare:117; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:218381928-218382047 | Common:1; Rare:17 | ||||
| chr2:218382062-218382354 | Rare:58 | ||||
| chr2:218398102-218398245 | Common:1; Rare:50 | ||||
| chr2:218398545-218398767 | Common:4; Rare:83 | ||||
| chr2:218400280-218400612 | Common:10; Rare:121 | ||||
| chr2:218568307-218568592 | Common:2; Rare:74 | ||||
| chr2:218659600-218659757 | Rare:40 | ||||
| chr2:218671972-218672318 | Common:2; Rare:88 | ||||
| chr2:218744720-218744893 | Rare:30 | ||||
| chr2:218749162-218749331 | Rare:35 | ||||
| chr2:218782013-218782191 | Rare:38; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:218782635-218782683 | Common:1; Rare:10 |