Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:77919397-77919696 | Common:1; Rare:107; Clinvar:2; Clinvar (benign):1 | ||||
chr13:79405716-79405902 | Common:1; Rare:59 | ||||
chr13:79406219-79406309 | Common:1; Rare:29 | ||||
chr13:80340861-80341125 | Common:1; Rare:80 | ||||
chr13:93227280-93227347 | Rare:15; Clinvar:2 | ||||
chr13:95676828-95677258 | Common:4; Rare:166 | ||||
chr13:96053353-96053594 | Common:2; Rare:98 | ||||
chr13:97222190-97222407 | Rare:35 | ||||
chr13:99200668-99200903 | Common:6; Rare:111 | ||||
chr13:99307392-99307611 | Common:2; Rare:31 | ||||
chr13:100088901-100089134 | Rare:86; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr13:100674809-100675055 | Common:3; Rare:100 | ||||
chr13:102596792-102597127 | Common:1; Rare:136; Clinvar:1; Clinvar (benign):1 | ||||
chr13:102773766-102773852 | Rare:36 | ||||
chr13:106567616-106567837 | Rare:67 |