| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:207625703-207625796 | Rare:18 | ||||
| chr2:208025492-208025629 | Rare:35 | ||||
| chr2:208254019-208254517 | Common:1; Rare:109 | ||||
| chr2:208254979-208255244 | Common:2; Rare:68 | ||||
| chr2:208266083-208266406 | Common:7; Rare:108; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:209771900-209771934 | Rare:11 | ||||
| chr2:210002433-210002670 | Common:6; Rare:84 | ||||
| chr2:210170717-210170901 | Rare:73 | ||||
| chr2:210477535-210477699 | Rare:48 | ||||
| chr2:213284238-213284483 | Rare:79 | ||||
| chr2:214809634-214809990 | Common:3; Rare:128; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:215311901-215312139 | Common:8; Rare:96 | ||||
| chr2:215365502-215365736 | Rare:60 | ||||
| chr2:215375280-215375479 | Common:1; Rare:47 | ||||
| chr2:215435855-215435903 | Rare:5 |