Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:227339169-227339390 | Common:2; Rare:39 | ||||
chr2:230466157-230466345 | Common:3; Rare:42 | ||||
chr2:230510400-230510650 | Common:6; Rare:31 | ||||
chr2:230513210-230513609 | Common:3; Rare:49 | ||||
chr2:230520764-230520951 | Rare:23 | ||||
chr2:231514259-231514603 | Common:6; Rare:132 | ||||
chr2:233012540-233012656 | Common:1; Rare:18 | ||||
chr2:233719476-233719569 | Rare:38 | ||||
chr2:233746884-233747201 | Rare:66 | ||||
chr2:233760846-233761033 | Common:1; Rare:65; Clinvar:4; Clinvar (pathogenic):4 | ||||
chr2:237581997-237582056 | Rare:12 | ||||
chr2:238422249-238422408 | Common:1; Rare:28 | ||||
chr2:240872813-240873018 | Common:2; Rare:41; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr2:240874020-240874323 | Common:6; Rare:82; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):4 | ||||
chr2:240967415-240967572 | Rare:34 |