Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:32628067-32628118 | Rare:16 | ||||
chr2:36355508-36355854 | Common:2; Rare:139 | ||||
chr2:36355883-36356078 | Common:2; Rare:52 | ||||
chr2:36356512-36356558 | Rare:18 | ||||
chr2:37084293-37084559 | Common:3; Rare:100 | ||||
chr2:37231559-37231745 | Common:4; Rare:107; Clinvar:1; Clinvar (benign):4 | ||||
chr2:37925443-37925549 | Rare:42 | ||||
chr2:38076124-38076265 | Rare:33 | ||||
chr2:38875868-38876030 | Common:2; Rare:56 | ||||
chr2:39437244-39437469 | Common:2; Rare:83 | ||||
chr2:43226586-43226840 | Common:1; Rare:100 | ||||
chr2:43899228-43899523 | Rare:92; Clinvar:1 | ||||
chr2:44361479-44361969 | Common:3; Rare:154 | ||||
chr2:46073575-46073689 | Common:1; Rare:16 | ||||
chr2:46616969-46617286 | Common:7; Rare:134 |