Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:39199982-39200352 | Common:3; Rare:114 | ||||
chr17:40342037-40342403 | Common:1; Rare:81 | ||||
chr17:41688935-41689023 | Common:2; Rare:44 | ||||
chr17:41812604-41813007 | Common:3; Rare:84; Clinvar:5 | ||||
chr17:42423139-42423397 | Common:1; Rare:69; Clinvar:2 | ||||
chr17:42536160-42536275 | Rare:36; Clinvar:2; Clinvar (pathogenic):2 | ||||
chr17:42577653-42577802 | Rare:70 | ||||
chr17:42609296-42609701 | Common:9; Rare:171; Clinvar (benign):1 | ||||
chr17:42761090-42761257 | Rare:48 | ||||
chr17:42964442-42964508 | Rare:29 | ||||
chr17:43170205-43170479 | Common:2; Rare:61 | ||||
chr17:43170983-43171227 | Rare:78 | ||||
chr17:44070612-44070954 | Common:3; Rare:121; Clinvar:4; Clinvar (benign):2 | ||||
chr17:44186715-44187044 | Rare:102 | ||||
chr17:44187153-44187310 | Common:1; Rare:39 |