Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:7961518-7961757 | Common:3; Rare:80; Clinvar:2; Clinvar (benign):3 | ||||
chr1:8026169-8026495 | Common:3; Rare:147 | ||||
chr1:8364810-8364863 | Rare:8 | ||||
chr1:8703085-8703173 | Rare:32 | ||||
chr1:8878583-8878852 | Rare:140 | ||||
chr1:9943247-9943488 | Common:3; Rare:62 | ||||
chr1:10032763-10032965 | Rare:53 | ||||
chr1:10398679-10399103 | Common:3; Rare:143 | ||||
chr1:10796574-10796849 | Common:3; Rare:83 | ||||
chr1:11099827-11099918 | Common:1; Rare:35 | ||||
chr1:11262484-11262776 | Common:2; Rare:92 | ||||
chr1:11654391-11654429 | Rare:6 | ||||
chr1:11654709-11654909 | Common:4; Rare:57 | ||||
chr1:11736026-11736235 | Common:3; Rare:63 | ||||
chr1:11805900-11806265 | Common:2; Rare:100; Clinvar:1 |