Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:52406080-52406262 | Common:5; Rare:44 | ||||
chr13:52450571-52450644 | Rare:22 | ||||
chr13:52455294-52455563 | Common:3; Rare:97 | ||||
chr13:52652543-52652926 | Common:3; Rare:113 | ||||
chr13:60163762-60164118 | Common:2; Rare:92 | ||||
chr13:67230317-67230509 | Common:1; Rare:63 | ||||
chr13:72727591-72727972 | Common:4; Rare:147 | ||||
chr13:72781841-72782261 | Common:1; Rare:149 | ||||
chr13:76886406-76886668 | Common:2; Rare:82 | ||||
chr13:76991988-76992181 | Common:2; Rare:92; Clinvar:16; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
chr13:77027137-77027264 | Common:5; Rare:43 | ||||
chr13:77918782-77918887 | Rare:23 | ||||
chr13:78659107-78659243 | Common:2; Rare:98 | ||||
chr13:79405776-79405882 | Rare:41 | ||||
chr13:79406219-79406295 | Common:1; Rare:19 |