| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:47335236-47335319 | Rare:16 | ||||
| chr2:47906506-47906815 | Common:2; Rare:103 | ||||
| chr2:55282245-55282362 | Common:5; Rare:38 | ||||
| chr2:64360113-64360273 | Rare:33 | ||||
| chr2:70086254-70086475 | Common:4; Rare:90 | ||||
| chr2:88016539-88016817 | Common:10; Rare:119 | ||||
| chr2:131682380-131682537 | Common:3; Rare:47 | ||||
| chr2:156254893-156254974 | Common:3; Rare:31 | ||||
| chr2:160270302-160270623 | Common:2; Rare:76 | ||||
| chr2:170770762-170771101 | Common:2; Rare:59 | ||||
| chr2:176637532-176637749 | Common:2; Rare:72 | ||||
| chr2:178605679-178605874 | Rare:42; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr2:188969438-188969507 | Rare:8 | ||||
| chr2:188977157-188977249 | Common:1; Rare:12 | ||||
| chr2:188985446-188985732 | Common:2; Rare:60; Clinvar (benign):1 |