Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:149163683-149163741 | Rare:13 | ||||
chr2:159042059-159042356 | Common:1; Rare:62 | ||||
chr2:159156907-159157087 | Rare:40 | ||||
chr2:160648335-160648493 | Common:1; Rare:44 | ||||
chr2:170770796-170771058 | Common:1; Rare:44 | ||||
chr2:172484540-172484905 | Rare:60 | ||||
chr2:178304400-178304454 | Common:1; Rare:5 | ||||
chr2:178304457-178304607 | Rare:30 | ||||
chr2:181773702-181773840 | Rare:25 | ||||
chr2:186173816-186174170 | Common:1; Rare:54 | ||||
chr2:202376105-202376219 | Rare:66 | ||||
chr2:214970326-214970469 | Common:1; Rare:41; Clinvar:1; Clinvar (benign):2 | ||||
chr2:214974821-214974913 | Common:1; Rare:18; Clinvar:1; Clinvar (benign):1 | ||||
chr2:214975942-214976169 | Common:1; Rare:58; Clinvar:1 | ||||
chr2:218272479-218272617 | Rare:47 |