Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:26221798-26221932 | Rare:35 | ||||
chr13:27251253-27251608 | Common:4; Rare:105 | ||||
chr13:28658952-28659175 | Rare:101; Clinvar (pathogenic):1 | ||||
chr13:30617579-30617993 | Common:1; Rare:126 | ||||
chr13:37000772-37000805 | Rare:17 | ||||
chr13:40771182-40771346 | Common:3; Rare:39 | ||||
chr13:41061352-41061558 | Common:2; Rare:64 | ||||
chr13:43879729-43879910 | Common:18; Rare:55 | ||||
chr13:44989449-44989576 | Rare:46 | ||||
chr13:45120396-45120560 | Common:1; Rare:54 | ||||
chr13:45341200-45341510 | Common:4; Rare:132 | ||||
chr13:46052696-46052865 | Common:2; Rare:48 | ||||
chr13:49495890-49496004 | Rare:21 | ||||
chr13:50081973-50082262 | Common:1; Rare:79 | ||||
chr13:52455335-52455503 | Common:3; Rare:55 |