Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:39037893-39038463 | Common:2; Rare:150 | ||||
chr13:40666586-40666805 | Common:2; Rare:80 | ||||
chr13:40771145-40771344 | Common:3; Rare:62 | ||||
chr13:40789355-40789635 | Common:2; Rare:94; Clinvar:6; Clinvar (benign):2 | ||||
chr13:40982858-40982950 | Common:1; Rare:14 | ||||
chr13:41060883-41061594 | Common:20; Rare:281 | ||||
chr13:41132781-41132974 | Rare:51 | ||||
chr13:42271720-42272038 | Common:2; Rare:88 | ||||
chr13:43879484-43879544 | Rare:14 | ||||
chr13:43879691-43879910 | Common:18; Rare:62 | ||||
chr13:44989456-44989610 | Rare:53 | ||||
chr13:45120372-45120475 | Common:2; Rare:28 | ||||
chr13:45341040-45341611 | Common:4; Rare:258 | ||||
chr13:45418329-45418578 | Rare:76 | ||||
chr13:45464878-45464925 | Rare:11 |