Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:50373168-50373242 | Common:2; Rare:30 | ||||
chr17:50719469-50719647 | Rare:68 | ||||
chr17:51166274-51166502 | Common:2; Rare:49 | ||||
chr17:54968631-54968792 | Common:3; Rare:77 | ||||
chr17:56914022-56914168 | Rare:36 | ||||
chr17:57850013-57850274 | Common:1; Rare:80 | ||||
chr17:58692541-58692663 | Common:1; Rare:67; Clinvar:9; Clinvar (benign):19 | ||||
chr17:59106727-59107175 | Common:2; Rare:147; Clinvar:4; Clinvar (benign):2 | ||||
chr17:59155138-59155763 | Common:2; Rare:155 | ||||
chr17:59619569-59619953 | Common:3; Rare:137 | ||||
chr17:59707392-59707713 | Common:3; Rare:92; Clinvar (benign):4 | ||||
chr17:59892877-59893140 | Rare:76 | ||||
chr17:60078912-60078974 | Common:4; Rare:33 | ||||
chr17:63773492-63773818 | Common:2; Rare:109 | ||||
chr17:64662305-64662413 | Common:1; Rare:47 |