Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:87155248-87155615 | Rare:100 | ||||
chr6:87589946-87590165 | Common:2; Rare:100; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr6:87702219-87702517 | Common:1; Rare:92 | ||||
chr6:88963540-88963826 | Common:2; Rare:95 | ||||
chr6:89117926-89118097 | Common:1; Rare:69 | ||||
chr6:89638438-89638606 | Common:1; Rare:34 | ||||
chr6:89638713-89638764 | Rare:21 | ||||
chr6:89819724-89819814 | Rare:34 | ||||
chr6:89829603-89829929 | Rare:79 | ||||
chr6:93419552-93419808 | Common:1; Rare:68 | ||||
chr6:95577408-95577571 | Common:4; Rare:45 | ||||
chr6:96521719-96521883 | Common:3; Rare:78 | ||||
chr6:96897798-96898099 | Common:4; Rare:111; Clinvar:4; Clinvar (benign):1 | ||||
chr6:99424874-99424980 | Rare:42 | ||||
chr6:99425253-99425506 | Common:2; Rare:69 |