Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:38686874-38687109 | Common:3; Rare:68; Clinvar:3; Clinvar (benign):1 | ||||
chr13:40982862-40983032 | Common:3; Rare:27 | ||||
chr13:41061395-41061633 | Common:2; Rare:70 | ||||
chr13:41132800-41132980 | Rare:45 | ||||
chr13:41457283-41457547 | Common:2; Rare:77 | ||||
chr13:42271964-42272190 | Common:2; Rare:50 | ||||
chr13:43879492-43879600 | Rare:32 | ||||
chr13:43879743-43879839 | Common:13; Rare:39 | ||||
chr13:44435170-44435452 | Common:3; Rare:81 | ||||
chr13:44989437-44989607 | Rare:64 | ||||
chr13:45120392-45120597 | Common:1; Rare:65 | ||||
chr13:45341040-45341609 | Common:4; Rare:258 | ||||
chr13:46052709-46052816 | Common:1; Rare:30 | ||||
chr13:48001246-48001405 | Common:1; Rare:74; Clinvar:3; Clinvar (benign):4 | ||||
chr13:48533049-48533094 | Rare:13 |