Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:50355058-50355585 | Common:3; Rare:214 | ||||
chr15:50424123-50424509 | Common:2; Rare:139 | ||||
chr15:50686674-50686937 | Common:5; Rare:105 | ||||
chr15:50765477-50765756 | Common:3; Rare:97 | ||||
chr15:50908577-50908772 | Common:2; Rare:81; Clinvar (benign):2 | ||||
chr15:51622715-51623061 | Common:3; Rare:119 | ||||
chr15:51751491-51751694 | Common:1; Rare:54 | ||||
chr15:51862990-51863024 | Rare:14 | ||||
chr15:51924260-51924397 | Common:1; Rare:25 | ||||
chr15:51971704-51971831 | Rare:64 | ||||
chr15:52019089-52019279 | Common:1; Rare:96 | ||||
chr15:52179668-52180047 | Common:1; Rare:132 | ||||
chr15:52678206-52678402 | Rare:45 | ||||
chr15:52678522-52678670 | Rare:38 | ||||
chr15:52678941-52679244 | Common:1; Rare:58 |