| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:210002443-210002659 | Common:5; Rare:74 | ||||
| chr2:210476666-210476845 | Rare:58 | ||||
| chr2:210477582-210477687 | Rare:36 | ||||
| chr2:213284218-213284486 | Rare:87 | ||||
| chr2:215311970-215312133 | Common:7; Rare:71 | ||||
| chr2:215375627-215375899 | Common:2; Rare:73 | ||||
| chr2:215409568-215410031 | Rare:129 | ||||
| chr2:215436023-215436261 | Common:2; Rare:75 | ||||
| chr2:216081771-216081929 | Common:1; Rare:56 | ||||
| chr2:216412261-216412561 | Common:3; Rare:69; Clinvar (benign):2 | ||||
| chr2:216498732-216498894 | Common:6; Rare:70 | ||||
| chr2:216694527-216694661 | Rare:31 | ||||
| chr2:217842166-217842294 | Common:1; Rare:32 | ||||
| chr2:218216988-218217226 | Common:2; Rare:84 | ||||
| chr2:218269713-218269750 | Rare:14 |