Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:40771141-40771333 | Common:3; Rare:56 | ||||
chr13:40789377-40789615 | Common:2; Rare:78; Clinvar:5; Clinvar (benign):2 | ||||
chr13:41060935-41061068 | Common:7; Rare:65 | ||||
chr13:41061356-41061594 | Common:2; Rare:69 | ||||
chr13:43879476-43879600 | Rare:37 | ||||
chr13:43879661-43879913 | Common:18; Rare:67 | ||||
chr13:44436808-44437033 | Common:2; Rare:71 | ||||
chr13:44989443-44989607 | Rare:62 | ||||
chr13:45120377-45120668 | Common:2; Rare:97 | ||||
chr13:45341040-45341609 | Common:4; Rare:258 | ||||
chr13:46052716-46052899 | Common:2; Rare:55 | ||||
chr13:48001256-48001385 | Common:1; Rare:61; Clinvar:3; Clinvar (benign):3 | ||||
chr13:48303721-48303880 | Rare:49; Clinvar:3 | ||||
chr13:48976396-48976662 | Common:3; Rare:94 | ||||
chr13:49247830-49247954 | Rare:34 |