Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:34961495-34961561 | Rare:32 | ||||
chr17:34980325-34980588 | Common:4; Rare:77 | ||||
chr17:35242957-35243100 | Rare:46 | ||||
chr17:35578545-35578684 | Common:1; Rare:32; Clinvar (benign):1 | ||||
chr17:36534772-36534998 | Common:3; Rare:92 | ||||
chr17:36544818-36544968 | Common:2; Rare:48 | ||||
chr17:37406799-37406924 | Rare:50 | ||||
chr17:37489709-37489919 | Rare:80 | ||||
chr17:37491416-37491531 | Common:2; Rare:27 | ||||
chr17:37609362-37609524 | Rare:67 | ||||
chr17:38706096-38706122 | Rare:12 | ||||
chr17:38749807-38749869 | Rare:14 | ||||
chr17:38825270-38825414 | Common:2; Rare:44 | ||||
chr17:39401619-39401816 | Common:1; Rare:53 | ||||
chr17:39451245-39451373 | Common:2; Rare:45 |