Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:132401338-132401637 | Common:3; Rare:96 | ||||
chr6:133889048-133889124 | Rare:7 | ||||
chr6:133952949-133953252 | Common:2; Rare:82 | ||||
chr6:134174855-134175004 | Common:1; Rare:64 | ||||
chr6:135054783-135054973 | Common:6; Rare:55 | ||||
chr6:135497604-135497860 | Common:4; Rare:94; Clinvar:1; Clinvar (benign):2 | ||||
chr6:136289774-136290063 | Common:2; Rare:129 | ||||
chr6:138773661-138773813 | Common:3; Rare:73 | ||||
chr6:142147187-142147287 | Rare:40 | ||||
chr6:143060724-143060928 | Common:7; Rare:72 | ||||
chr6:143450667-143450961 | Common:1; Rare:108; Clinvar:4; Clinvar (benign):1 | ||||
chr6:145814666-145814921 | Common:1; Rare:114 | ||||
chr6:149545994-149546191 | Common:1; Rare:85 | ||||
chr6:149749647-149749796 | Rare:85 | ||||
chr6:149963813-149964007 | Common:1; Rare:55 |