Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:69339556-69339824 | Common:1; Rare:110; Clinvar (benign):1 | ||||
chr16:70523537-70523822 | Common:3; Rare:88 | ||||
chr16:75647652-75647809 | Common:2; Rare:70 | ||||
chr16:88856908-88857133 | Common:4; Rare:100; Clinvar:1; Clinvar (benign):2 | ||||
chr17:15999645-15999760 | Common:1; Rare:64; Clinvar:2; Clinvar (benign):3 | ||||
chr17:18314981-18315277 | Rare:87 | ||||
chr17:28357474-28357647 | Common:5; Rare:80 | ||||
chr17:45061129-45061329 | Common:1; Rare:59 | ||||
chr17:59707401-59707722 | Common:3; Rare:89; Clinvar (benign):3 | ||||
chr17:63741791-63741983 | Common:3; Rare:87 | ||||
chr17:67717685-67717935 | Common:1; Rare:77 | ||||
chr17:75046945-75047077 | Rare:33 | ||||
chr17:75261598-75261898 | Common:3; Rare:83 | ||||
chr17:75979162-75979271 | Rare:30; Clinvar:3 | ||||
chr19:8321358-8321497 | Common:2; Rare:54 |