Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:5191838-5192112 | Common:2; Rare:88 | ||||
chr17:5234814-5234983 | Rare:36 | ||||
chr17:5419639-5419881 | Common:3; Rare:73 | ||||
chr17:5420017-5420222 | Rare:83 | ||||
chr17:5438864-5439002 | Rare:43 | ||||
chr17:5486157-5486581 | Common:5; Rare:143 | ||||
chr17:5486789-5486920 | Common:4; Rare:40 | ||||
chr17:6640646-6641084 | Common:7; Rare:134 | ||||
chr17:6651542-6651643 | Common:1; Rare:36 | ||||
chr17:7012317-7012738 | Rare:135 | ||||
chr17:7219735-7219944 | Common:3; Rare:84; Clinvar:5; Clinvar (benign):1 | ||||
chr17:7224438-7224884 | Common:2; Rare:156; Clinvar:12; Clinvar (benign):19; Clinvar (pathogenic):4 | ||||
chr17:7251963-7252574 | Common:3; Rare:228 | ||||
chr17:7313378-7313623 | Common:1; Rare:99 | ||||
chr17:7351630-7351738 | Rare:19 |