Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:37059590-37059741 | Common:1; Rare:51 | ||||
chr13:38350214-38350287 | Rare:37 | ||||
chr13:39037753-39037856 | Rare:34 | ||||
chr13:39038064-39038495 | Common:1; Rare:104 | ||||
chr13:40771029-40771344 | Common:3; Rare:109 | ||||
chr13:40789341-40789617 | Common:2; Rare:92; Clinvar:5; Clinvar (benign):2 | ||||
chr13:41019229-41019451 | Rare:34 | ||||
chr13:41060846-41061641 | Common:20; Rare:324 | ||||
chr13:41061736-41061839 | Common:1; Rare:35 | ||||
chr13:41132725-41132984 | Rare:72 | ||||
chr13:42271777-42272190 | Common:4; Rare:109 | ||||
chr13:43879467-43879925 | Common:19; Rare:121 | ||||
chr13:44989428-44989721 | Rare:113 | ||||
chr13:45120377-45120682 | Common:2; Rare:100 | ||||
chr13:45341036-45341630 | Common:4; Rare:267 |