Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:40821935-40822681 | Common:3; Rare:218; Clinvar:2; Clinvar (pathogenic):2 | ||||
chr17:41586308-41586965 | Common:9; Rare:242; Clinvar:7; Clinvar (benign):7; Clinvar (pathogenic):4 | ||||
chr17:41688642-41689066 | Common:3; Rare:169 | ||||
chr17:41785957-41786216 | Common:1; Rare:51 | ||||
chr17:42017382-42017511 | Common:1; Rare:55 | ||||
chr17:42154930-42155281 | Common:4; Rare:95 | ||||
chr17:42423014-42423080 | Rare:28; Clinvar:1 | ||||
chr17:42423083-42423290 | Rare:58; Clinvar:2 | ||||
chr17:42577682-42577844 | Rare:77 | ||||
chr17:42609330-42609732 | Common:8; Rare:167; Clinvar (benign):2 | ||||
chr17:42761005-42761254 | Rare:66 | ||||
chr17:42833338-42833547 | Rare:68 | ||||
chr17:43011971-43012210 | Common:2; Rare:54 | ||||
chr17:43125466-43125662 | Rare:45; Clinvar (benign):1 | ||||
chr17:43170297-43170720 | Common:3; Rare:83 |