Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:77320077-77320324 | Common:1; Rare:65; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr17:78187045-78187376 | Common:3; Rare:106 | ||||
chr17:78840745-78841004 | Common:2; Rare:93 | ||||
chr17:79023821-79024179 | Common:1; Rare:78 | ||||
chr17:80035830-80035994 | Common:1; Rare:57 | ||||
chr17:80147121-80147345 | Common:5; Rare:88 | ||||
chr17:80220309-80220453 | Rare:57; Clinvar:1; Clinvar (pathogenic):2 | ||||
chr17:80415095-80415189 | Common:1; Rare:61 | ||||
chr17:80415420-80415509 | Common:4; Rare:37 | ||||
chr17:81636922-81637232 | Common:2; Rare:126 | ||||
chr17:81666554-81666769 | Common:1; Rare:95 | ||||
chr17:81683641-81684076 | Common:5; Rare:228 | ||||
chr17:81703283-81703513 | Common:2; Rare:65; Clinvar (benign):2 | ||||
chr17:81833243-81833380 | Rare:60 | ||||
chr17:81869962-81870263 | Common:1; Rare:78 |