Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:40341181-40341191 | |||||
chr17:40342037-40342400 | Common:1; Rare:80 | ||||
chr17:41688633-41688966 | Common:1; Rare:133 | ||||
chr17:41689287-41689561 | Common:3; Rare:103 | ||||
chr17:41786656-41786830 | Common:2; Rare:49; Clinvar (benign):1 | ||||
chr17:41812621-41813029 | Common:3; Rare:91; Clinvar:5 | ||||
chr17:41835995-41836312 | Common:2; Rare:87 | ||||
chr17:41930521-41930676 | Rare:43 | ||||
chr17:42017114-42017216 | Rare:18 | ||||
chr17:42017382-42017486 | Rare:47 | ||||
chr17:42017577-42017814 | Rare:62 | ||||
chr17:42121338-42121467 | Rare:30 | ||||
chr17:42154910-42155152 | Common:3; Rare:64 | ||||
chr17:42388337-42388887 | Common:1; Rare:151; Clinvar:3 | ||||
chr17:42423093-42423399 | Common:1; Rare:81; Clinvar:2 |