Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:41060941-41061008 | Common:5; Rare:34 | ||||
chr13:41061395-41061579 | Common:2; Rare:49 | ||||
chr13:41311189-41311330 | Common:1; Rare:63 | ||||
chr13:43879743-43879913 | Common:15; Rare:53 | ||||
chr13:44436800-44436997 | Common:2; Rare:61 | ||||
chr13:44989408-44989607 | Rare:83 | ||||
chr13:45341040-45341609 | Common:4; Rare:258 | ||||
chr13:45464822-45464995 | Rare:46 | ||||
chr13:46052716-46052842 | Common:2; Rare:33 | ||||
chr13:48037505-48037767 | Rare:101 | ||||
chr13:48303674-48303894 | Rare:73; Clinvar:3; Clinvar (pathogenic):1 | ||||
chr13:48533078-48533129 | Common:1; Rare:16 | ||||
chr13:48975800-48975928 | Rare:48 | ||||
chr13:48976343-48976662 | Common:3; Rare:106 | ||||
chr13:49247830-49247976 | Rare:45 |