Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:131492292-131492446 | Common:3; Rare:66 | ||||
chr2:131493047-131493097 | Common:1; Rare:13 | ||||
chr2:134918641-134918894 | Common:1; Rare:114 | ||||
chr2:138501675-138501866 | Common:1; Rare:80 | ||||
chr2:148020692-148021096 | Common:2; Rare:94; Clinvar (benign):2 | ||||
chr2:148021484-148021676 | Rare:48 | ||||
chr2:149587318-149587358 | Rare:8 | ||||
chr2:149587696-149587827 | Common:1; Rare:38; Clinvar:1 | ||||
chr2:152717850-152717977 | Rare:53 | ||||
chr2:159712348-159712534 | Common:2; Rare:74 | ||||
chr2:162073555-162073689 | Rare:33 | ||||
chr2:162318656-162318794 | Rare:29 | ||||
chr2:171433967-171434248 | Common:2; Rare:69 | ||||
chr2:174248452-174248752 | Common:1; Rare:92 | ||||
chr2:174395663-174395795 | Common:1; Rare:40 |