Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:32142359-32142599 | Common:7; Rare:112 | ||||
chr17:32350017-32350189 | Rare:89 | ||||
chr17:34961456-34961585 | Common:1; Rare:64 | ||||
chr17:34980382-34980597 | Common:4; Rare:63 | ||||
chr17:34981146-34981450 | Common:2; Rare:60 | ||||
chr17:35242910-35243087 | Rare:60 | ||||
chr17:35578539-35578702 | Common:1; Rare:42; Clinvar (benign):1 | ||||
chr17:35587231-35587551 | Rare:79 | ||||
chr17:36534825-36535034 | Common:3; Rare:97 | ||||
chr17:36544790-36544968 | Common:3; Rare:58 | ||||
chr17:37406812-37406929 | Rare:44 | ||||
chr17:37489709-37489894 | Rare:74 | ||||
chr17:37609362-37609561 | Common:1; Rare:87 | ||||
chr17:37745057-37745208 | Rare:36; Clinvar (benign):2 | ||||
chr17:38705118-38705306 | Common:1; Rare:55 |