Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:42017106-42017576 | Common:1; Rare:145 | ||||
chr17:42017581-42017678 | Rare:29 | ||||
chr17:42018482-42018804 | Common:1; Rare:60 | ||||
chr17:42019932-42020155 | Common:1; Rare:66 | ||||
chr17:42121312-42121382 | Common:1; Rare:29 | ||||
chr17:42194407-42194575 | Rare:32 | ||||
chr17:42276284-42276496 | Rare:83 | ||||
chr17:42316984-42317183 | Common:3; Rare:28; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr17:42423214-42423514 | Common:1; Rare:80; Clinvar:1 | ||||
chr17:42458738-42458936 | Common:3; Rare:75 | ||||
chr17:42536137-42536287 | Rare:44; Clinvar:2; Clinvar (pathogenic):2 | ||||
chr17:42566974-42567274 | Common:4; Rare:94 | ||||
chr17:42577667-42577832 | Rare:80 | ||||
chr17:42609307-42609784 | Common:8; Rare:192; Clinvar (benign):2 | ||||
chr17:42659157-42659434 | Rare:86 |