Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:51789568-51789777 | Rare:55 | ||||
chr1:51878525-51878949 | Common:2; Rare:131 | ||||
chr1:52055084-52055271 | Common:1; Rare:53 | ||||
chr1:52056169-52056378 | Rare:56 | ||||
chr1:52356186-52356425 | Rare:87 | ||||
chr1:52366101-52366291 | Common:1; Rare:56 | ||||
chr1:52404405-52404635 | Common:1; Rare:68 | ||||
chr1:52553033-52553386 | Common:4; Rare:102 | ||||
chr1:52553444-52553697 | Common:3; Rare:72 | ||||
chr1:52602308-52602510 | Common:2; Rare:62 | ||||
chr1:52698070-52698226 | Common:1; Rare:43 | ||||
chr1:52913989-52914209 | Rare:51 | ||||
chr1:52927164-52927359 | Common:4; Rare:62 | ||||
chr1:53062106-53062298 | Common:5; Rare:51 | ||||
chr1:53196691-53196824 | Rare:47; Clinvar:2; Clinvar (benign):1 |