Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:177164684-177164936 | Rare:57 | ||||
chr1:178725011-178725320 | Common:10; Rare:107 | ||||
chr1:179877766-179877872 | Rare:23 | ||||
chr1:179882223-179882311 | Rare:16 | ||||
chr1:179882493-179882860 | Rare:176; Clinvar:7; Clinvar (benign):2 | ||||
chr1:179954447-179954834 | Common:3; Rare:91 | ||||
chr1:180502492-180502757 | Common:2; Rare:109 | ||||
chr1:181482291-181482934 | Common:3; Rare:186 | ||||
chr1:182391776-182391969 | Common:2; Rare:58; Clinvar:1; Clinvar (benign):2 | ||||
chr1:182789587-182789776 | Common:2; Rare:58 | ||||
chr1:182839041-182839389 | Common:1; Rare:114 | ||||
chr1:183418259-183418435 | Rare:39 | ||||
chr1:183635638-183636123 | Common:5; Rare:137 | ||||
chr1:184386728-184387158 | Common:3; Rare:125 | ||||
chr1:185156941-185157314 | Common:1; Rare:102 |