Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:24922803-24923108 | Common:2; Rare:106; Clinvar:1 | ||||
chr13:25301492-25301692 | Common:1; Rare:79 | ||||
chr13:26221792-26221995 | Rare:60 | ||||
chr13:26222259-26222554 | Common:5; Rare:74 | ||||
chr13:27251245-27251617 | Common:6; Rare:112 | ||||
chr13:27450127-27450215 | Common:3; Rare:27 | ||||
chr13:28658881-28659194 | Common:1; Rare:121; Clinvar (pathogenic):1 | ||||
chr13:33285687-33285998 | Common:1; Rare:64 | ||||
chr13:36346301-36346499 | Common:3; Rare:57; Clinvar:3; Clinvar (benign):2 | ||||
chr13:37000736-37000808 | Rare:29 | ||||
chr13:37059600-37059746 | Common:1; Rare:49 | ||||
chr13:39603109-39603286 | Common:1; Rare:59 | ||||
chr13:41061194-41061579 | Common:3; Rare:132 | ||||
chr13:43879464-43879615 | Rare:42 | ||||
chr13:43879718-43879920 | Common:18; Rare:59 |