Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:10697516-10697644 | Common:3; Rare:45; Clinvar:2; Clinvar (benign):2 | ||||
chr17:14069463-14069525 | Common:1; Rare:21; Clinvar (benign):2 | ||||
chr17:15999641-15999829 | Common:1; Rare:100; Clinvar:4; Clinvar (benign):4 | ||||
chr17:16215527-16215632 | Rare:46 | ||||
chr17:16217102-16217232 | Rare:34; Clinvar:1 | ||||
chr17:16381022-16381163 | Common:3; Rare:70 | ||||
chr17:18039164-18039412 | Common:2; Rare:65 | ||||
chr17:18183748-18183925 | Rare:80 | ||||
chr17:18314925-18315324 | Common:1; Rare:113 | ||||
chr17:19362565-19362775 | Common:2; Rare:97; Clinvar:1; Clinvar (benign):2 | ||||
chr17:21214137-21214357 | Common:2; Rare:98 | ||||
chr17:28335383-28335689 | Common:1; Rare:71 | ||||
chr17:28357467-28357667 | Common:5; Rare:99 | ||||
chr17:28661895-28662271 | Common:1; Rare:131 | ||||
chr17:29568505-29568740 | Common:3; Rare:76 |