| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:177264630-177264905 | Common:2; Rare:83 | ||||
| chr2:177392657-177392808 | Common:1; Rare:40; Clinvar:1 | ||||
| chr2:177552761-177553052 | Common:4; Rare:89 | ||||
| chr2:178072766-178072914 | Rare:37 | ||||
| chr2:178451090-178451310 | Common:5; Rare:68; Clinvar:4; Clinvar (benign):3 | ||||
| chr2:178478515-178478644 | Common:1; Rare:41 | ||||
| chr2:182715935-182716328 | Common:3; Rare:137 | ||||
| chr2:186485994-186486360 | Common:3; Rare:106 | ||||
| chr2:188291735-188292060 | Common:4; Rare:93 | ||||
| chr2:188292469-188292936 | Common:2; Rare:105 | ||||
| chr2:189007933-189008142 | Rare:71; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):13 | ||||
| chr2:189179701-189179842 | Rare:15; Clinvar:1 | ||||
| chr2:189441086-189441166 | Rare:27 | ||||
| chr2:189580754-189580925 | Common:1; Rare:53; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:189784275-189784506 | Common:3; Rare:75; Clinvar:7; Clinvar (benign):1 |