Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:2511752-2511995 | Common:2; Rare:64 | ||||
chr17:2593357-2593734 | Common:5; Rare:137; Clinvar:2; Clinvar (benign):2 | ||||
chr17:2593750-2594001 | Common:1; Rare:63; Clinvar:4; Clinvar (benign):3 | ||||
chr17:2711721-2711944 | Common:1; Rare:70 | ||||
chr17:2776663-2776923 | Common:5; Rare:75 | ||||
chr17:3636193-3636489 | Common:4; Rare:93; Clinvar (benign):1 | ||||
chr17:3636622-3636789 | Common:1; Rare:40; Clinvar:3; Clinvar (benign):1 | ||||
chr17:3668433-3668829 | Common:3; Rare:163 | ||||
chr17:3723767-3723936 | Common:1; Rare:98 | ||||
chr17:3845897-3845999 | Rare:21 | ||||
chr17:3846208-3846458 | Common:1; Rare:77 | ||||
chr17:3892946-3893189 | Common:3; Rare:79 | ||||
chr17:4142954-4143230 | Common:3; Rare:96 | ||||
chr17:4143595-4143758 | Common:4; Rare:96 | ||||
chr17:4263934-4264115 | Rare:71 |