Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:50196153-50196368 | Common:1; Rare:68; Clinvar:2; Clinvar (benign):2 | ||||
chr17:50198160-50198504 | Common:1; Rare:74; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr17:50199554-50199954 | Common:7; Rare:133; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr17:50345905-50346140 | Common:4; Rare:81 | ||||
chr17:50373168-50373250 | Common:3; Rare:34 | ||||
chr17:50719469-50719700 | Rare:93 | ||||
chr17:50866337-50866616 | Common:3; Rare:84 | ||||
chr17:51166274-51166557 | Common:2; Rare:65 | ||||
chr17:51260137-51260587 | Common:3; Rare:166 | ||||
chr17:54968589-54968799 | Common:3; Rare:97 | ||||
chr17:56914022-56914186 | Rare:43 | ||||
chr17:57084986-57085328 | Rare:116 | ||||
chr17:57850006-57850270 | Common:1; Rare:86 | ||||
chr17:57988162-57988525 | Common:5; Rare:108 | ||||
chr17:58007130-58007380 | Common:1; Rare:119 |