| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:216695111-216695291 | Common:2; Rare:28 | ||||
| chr2:218217047-218217291 | Common:2; Rare:80 | ||||
| chr2:218270109-218270343 | Common:5; Rare:66 | ||||
| chr2:218659597-218659746 | Rare:36 | ||||
| chr2:218671954-218672339 | Common:2; Rare:101 | ||||
| chr2:218710709-218710999 | Common:2; Rare:68 | ||||
| chr2:219176898-219177069 | Common:4; Rare:52 | ||||
| chr2:219229297-219229422 | Rare:37 | ||||
| chr2:219229544-219229793 | Common:1; Rare:73 | ||||
| chr2:219245391-219245540 | Common:1; Rare:45 | ||||
| chr2:219279024-219279545 | Common:3; Rare:147; Clinvar (benign):1 | ||||
| chr2:219498666-219498935 | Common:2; Rare:62 | ||||
| chr2:219543596-219544105 | Common:3; Rare:160 | ||||
| chr2:226795014-226795124 | Rare:46 | ||||
| chr2:227325191-227325371 | Common:5; Rare:60 |