Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:168136147-168136184 | Rare:11 | ||||
chr1:168136190-168136375 | Common:2; Rare:56; Clinvar (benign):1 | ||||
chr1:168136660-168136977 | Common:2; Rare:72 | ||||
chr1:168137160-168137315 | Rare:30 | ||||
chr1:168137324-168137462 | Common:2; Rare:29 | ||||
chr1:168178701-168179105 | Common:4; Rare:123 | ||||
chr1:168179145-168179619 | Common:1; Rare:109 | ||||
chr1:168225483-168225563 | Rare:14 | ||||
chr1:168225617-168225807 | Common:3; Rare:65 | ||||
chr1:168225848-168226146 | Common:3; Rare:102 | ||||
chr1:168226413-168226537 | Rare:36 | ||||
chr1:169105788-169105955 | Common:2; Rare:48 | ||||
chr1:169106107-169106493 | Common:5; Rare:140 | ||||
chr1:169106504-169106776 | Common:1; Rare:104 | ||||
chr1:169107507-169107614 | Rare:24 |