Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:633984-634051 | Rare:31 | ||||
chr1:778536-778929 | Common:5; Rare:138 | ||||
chr1:779126-779244 | Common:1; Rare:35 | ||||
chr1:827199-827303 | Common:4; Rare:21 | ||||
chr1:827316-827411 | Rare:20 | ||||
chr1:827433-827731 | Common:3; Rare:110 | ||||
chr1:904628-904872 | Common:4; Rare:86 | ||||
chr1:905341-905429 | Common:1; Rare:24 | ||||
chr1:1001883-1002006 | Rare:44 | ||||
chr1:1014345-1014553 | Common:3; Rare:88; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr1:1017578-1017643 | Rare:16 | ||||
chr1:1033034-1033433 | Common:1; Rare:107 | ||||
chr1:1038778-1039001 | Common:9; Rare:56 | ||||
chr1:1059288-1059431 | Common:3; Rare:38 | ||||
chr1:1059537-1059751 | Common:1; Rare:89 |