Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:5486157-5486387 | Common:4; Rare:104 | ||||
chr17:6640701-6641079 | Common:7; Rare:117 | ||||
chr17:7012332-7012680 | Rare:119 | ||||
chr17:7583564-7583858 | Common:1; Rare:120; Clinvar:3; Clinvar (benign):3 | ||||
chr17:10697503-10697648 | Common:3; Rare:55; Clinvar:2; Clinvar (benign):2 | ||||
chr17:14069467-14069529 | Common:1; Rare:21; Clinvar (benign):2 | ||||
chr17:28335396-28335815 | Common:1; Rare:99 | ||||
chr17:28645112-28645310 | Common:1; Rare:69 | ||||
chr17:28661883-28662234 | Common:1; Rare:116 | ||||
chr17:29294111-29294370 | Common:3; Rare:103 | ||||
chr17:35242948-35243076 | Rare:38 | ||||
chr17:37406820-37406913 | Rare:35 | ||||
chr17:38853706-38853888 | Common:3; Rare:75 | ||||
chr17:38869836-38870103 | Common:4; Rare:86 | ||||
chr17:39927544-39927777 | Common:2; Rare:72 |