Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:49463215-49463397 | Common:1; Rare:56; Clinvar (benign):1 | ||||
chr6:52420125-52420364 | Common:3; Rare:98; Clinvar:1; Clinvar (benign):2 | ||||
chr6:52995275-52995812 | Common:4; Rare:224 | ||||
chr6:53348904-53349222 | Common:2; Rare:113 | ||||
chr6:73520998-73521396 | Common:2; Rare:102 | ||||
chr6:73521560-73521625 | Rare:18 | ||||
chr6:73653922-73654169 | Common:3; Rare:68; Clinvar:3 | ||||
chr6:73696019-73696210 | Common:1; Rare:38 | ||||
chr6:75284715-75285014 | Common:1; Rare:89 | ||||
chr6:75601771-75601893 | Rare:48 | ||||
chr6:79537364-79537638 | Common:2; Rare:82; Clinvar:4 | ||||
chr6:81752675-81752847 | Rare:90 | ||||
chr6:83193194-83193407 | Common:3; Rare:72 | ||||
chr6:84764585-84764813 | Common:1; Rare:68 | ||||
chr6:85449895-85450116 | Common:1; Rare:64 |