Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:40417819-40418166 | Rare:101 | ||||
chr17:41812643-41813022 | Common:2; Rare:88; Clinvar:5 | ||||
chr17:41966610-41966837 | Common:1; Rare:82 | ||||
chr17:42017388-42017503 | Common:1; Rare:49 | ||||
chr17:42017577-42017725 | Rare:44 | ||||
chr17:42154952-42155265 | Common:3; Rare:82 | ||||
chr17:42423144-42423454 | Common:1; Rare:81; Clinvar:2 | ||||
chr17:42458735-42458920 | Common:1; Rare:71 | ||||
chr17:42566783-42567120 | Common:3; Rare:106 | ||||
chr17:42577631-42577834 | Rare:97 | ||||
chr17:42609333-42609756 | Common:8; Rare:174; Clinvar (benign):2 | ||||
chr17:42773369-42773476 | Rare:31 | ||||
chr17:42833096-42833497 | Rare:117 | ||||
chr17:42964428-42964534 | Rare:50 | ||||
chr17:43125324-43125662 | Rare:85; Clinvar:3; Clinvar (benign):3 |