Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:5486157-5486602 | Common:5; Rare:152 | ||||
chr17:5486810-5486917 | Common:3; Rare:33 | ||||
chr17:5584465-5584617 | Common:1; Rare:31 | ||||
chr17:6444238-6444468 | Common:2; Rare:71 | ||||
chr17:6640646-6641121 | Common:7; Rare:152 | ||||
chr17:6651574-6651747 | Common:1; Rare:53 | ||||
chr17:7012301-7012705 | Rare:135 | ||||
chr17:7315108-7315410 | Common:4; Rare:106 | ||||
chr17:7352054-7352207 | Rare:48 | ||||
chr17:7479562-7479709 | Rare:23 | ||||
chr17:7484207-7484380 | Common:1; Rare:74 | ||||
chr17:7583542-7583872 | Common:1; Rare:133; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr17:7584074-7584114 | Rare:8 | ||||
chr17:7687485-7687569 | Rare:22 | ||||
chr17:7857085-7857365 | Common:1; Rare:140 |