Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:35147631-35147905 | Common:1; Rare:56 | ||||
chr17:35242901-35243099 | Rare:65 | ||||
chr17:35373609-35373769 | Common:3; Rare:34 | ||||
chr17:35578496-35578699 | Common:1; Rare:53; Clinvar:1; Clinvar (benign):1 | ||||
chr17:36486477-36486721 | Common:3; Rare:86 | ||||
chr17:36534830-36535039 | Common:3; Rare:96 | ||||
chr17:36544781-36544968 | Common:3; Rare:64 | ||||
chr17:36545395-36545665 | Common:2; Rare:91 | ||||
chr17:37406812-37406929 | Rare:44 | ||||
chr17:37489721-37489909 | Rare:74 | ||||
chr17:37609317-37609561 | Common:1; Rare:100 | ||||
chr17:38428309-38428480 | Common:8; Rare:67 | ||||
chr17:38706095-38706141 | Rare:24 | ||||
chr17:38799387-38799749 | Common:2; Rare:120 | ||||
chr17:38825270-38825408 | Common:2; Rare:41 |