Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:31321590-31321886 | Common:3; Rare:48 | ||||
chr17:31936741-31937057 | Rare:88 | ||||
chr17:32142302-32142719 | Common:8; Rare:164 | ||||
chr17:32350012-32350318 | Rare:136 | ||||
chr17:33293264-33293486 | Rare:60 | ||||
chr17:34961444-34961569 | Common:1; Rare:60 | ||||
chr17:34981113-34981451 | Common:2; Rare:65 | ||||
chr17:35119814-35119917 | Rare:38; Clinvar:2; Clinvar (benign):1 | ||||
chr17:35242910-35243091 | Rare:60 | ||||
chr17:35578485-35578710 | Common:1; Rare:59; Clinvar:1; Clinvar (benign):1 | ||||
chr17:35587184-35587512 | Rare:88 | ||||
chr17:36534794-36535016 | Common:3; Rare:92 | ||||
chr17:36544775-36544997 | Common:4; Rare:75 | ||||
chr17:37406738-37406936 | Rare:79 | ||||
chr17:37489721-37489900 | Rare:71 |