Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:44573174-44573349 | Rare:62 | ||||
chr13:44573354-44573529 | Common:1; Rare:58 | ||||
chr13:44989443-44989634 | Rare:75 | ||||
chr13:45341040-45341610 | Common:4; Rare:258 | ||||
chr13:46052696-46052812 | Common:1; Rare:33 | ||||
chr13:48001225-48001379 | Common:1; Rare:71; Clinvar:3; Clinvar (benign):6 | ||||
chr13:48037662-48037795 | Common:1; Rare:71 | ||||
chr13:48303667-48303880 | Rare:71; Clinvar:3; Clinvar (pathogenic):1 | ||||
chr13:48975772-48975923 | Common:2; Rare:51 | ||||
chr13:49110247-49110380 | Common:1; Rare:39 | ||||
chr13:49247807-49247976 | Rare:48 | ||||
chr13:49444009-49444476 | Common:1; Rare:151 | ||||
chr13:49495930-49496055 | Rare:33 | ||||
chr13:49585524-49585612 | Common:1; Rare:27 | ||||
chr13:49936222-49936551 | Common:1; Rare:102 |