Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:60163865-60164062 | Common:1; Rare:44 | ||||
chr13:72727556-72727972 | Common:7; Rare:164 | ||||
chr13:72781836-72782188 | Common:1; Rare:135 | ||||
chr13:75549475-75549837 | Common:8; Rare:90 | ||||
chr13:75636033-75636366 | Common:2; Rare:76 | ||||
chr13:76992038-76992181 | Rare:68; Clinvar:9; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
chr13:79405795-79405885 | Rare:33 | ||||
chr13:79406217-79406339 | Common:3; Rare:38 | ||||
chr13:93227167-93227354 | Rare:40; Clinvar:2 | ||||
chr13:94601572-94601918 | Common:4; Rare:102 | ||||
chr13:95301395-95301589 | Rare:56 | ||||
chr13:95676930-95677177 | Common:3; Rare:84 | ||||
chr13:96053357-96053526 | Common:2; Rare:72 | ||||
chr13:97222134-97222358 | Rare:42 | ||||
chr13:99200667-99200894 | Common:6; Rare:104 |