Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:31958860-31959179 | Rare:99; Clinvar:8 | ||||
chr6:32153864-32154194 | Common:2; Rare:59 | ||||
chr6:32178106-32178412 | Common:2; Rare:43 | ||||
chr6:32843998-32844120 | Rare:28; Clinvar:1 | ||||
chr6:32853832-32854213 | Common:3; Rare:85 | ||||
chr6:33271862-33272085 | Rare:80 | ||||
chr6:42929218-42929549 | Common:3; Rare:90 | ||||
chr6:43013917-43014283 | Common:1; Rare:76 | ||||
chr6:43477406-43477587 | Rare:36 | ||||
chr6:43516890-43517106 | Common:3; Rare:84; Clinvar:2 | ||||
chr6:44127365-44127631 | Common:4; Rare:75 | ||||
chr6:46652778-46652975 | Rare:55 | ||||
chr6:83193222-83193364 | Common:3; Rare:52 | ||||
chr6:87589965-87590164 | Common:2; Rare:82; Clinvar (benign):3 | ||||
chr6:109382401-109382584 | Common:5; Rare:73; Clinvar (benign):1 |