| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:165794693-165794987 | Common:1; Rare:53 | ||||
| chr2:170928970-170929313 | Common:4; Rare:106 | ||||
| chr2:171433955-171434230 | Common:2; Rare:71 | ||||
| chr2:171522291-171522473 | Common:3; Rare:41 | ||||
| chr2:171894217-171894334 | Rare:56; Clinvar:1 | ||||
| chr2:171922304-171922506 | Rare:78 | ||||
| chr2:174248461-174248779 | Common:1; Rare:103 | ||||
| chr2:174395678-174395794 | Common:1; Rare:37 | ||||
| chr2:177212614-177212797 | Common:1; Rare:81 | ||||
| chr2:177264646-177264916 | Common:2; Rare:81 | ||||
| chr2:177392669-177392905 | Rare:85; Clinvar:5; Clinvar (benign):2 | ||||
| chr2:181457237-181457407 | Rare:58 | ||||
| chr2:182715935-182716323 | Common:3; Rare:136 | ||||
| chr2:186486158-186486344 | Common:2; Rare:55 | ||||
| chr2:189784289-189784461 | Common:2; Rare:50; Clinvar:6; Clinvar (benign):1 |