Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:70523533-70523829 | Common:3; Rare:95; Clinvar (pathogenic):1 | ||||
chr16:72093605-72093929 | Rare:74 | ||||
chr16:74296750-74296904 | Rare:64 | ||||
chr16:75647638-75647817 | Common:2; Rare:85; Clinvar:3 | ||||
chr16:81006839-81007195 | Common:3; Rare:118 | ||||
chr16:84116903-84117032 | Common:1; Rare:48 | ||||
chr16:88856932-88857148 | Common:4; Rare:94; Clinvar (benign):2 | ||||
chr16:89560462-89560725 | Common:1; Rare:125 | ||||
chr17:1516628-1516949 | Rare:111 | ||||
chr17:2336441-2336620 | Rare:64 | ||||
chr17:3668568-3668829 | Common:1; Rare:103 | ||||
chr17:4939924-4940101 | Common:1; Rare:57 | ||||
chr17:5419651-5419882 | Common:3; Rare:67 | ||||
chr17:5486166-5486519 | Common:4; Rare:123 | ||||
chr17:6640667-6641077 | Common:7; Rare:127 |