Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:67307236-67307401 | Rare:32 | ||||
chr1:67684914-67685247 | Common:3; Rare:87 | ||||
chr1:68497040-68497308 | Common:3; Rare:89 | ||||
chr1:70205542-70205759 | Rare:69 | ||||
chr1:70221307-70221655 | Rare:138 | ||||
chr1:70230516-70230631 | Rare:24 | ||||
chr1:70354668-70354811 | Rare:48 | ||||
chr1:71080991-71081364 | Rare:100 | ||||
chr1:72282707-72282987 | Common:5; Rare:91 | ||||
chr1:74198149-74198378 | Common:2; Rare:123 | ||||
chr1:74733001-74733152 | Common:4; Rare:44 | ||||
chr1:75724659-75724815 | Common:1; Rare:72; Clinvar:4; Clinvar (benign):1 | ||||
chr1:77219391-77219528 | Rare:63 | ||||
chr1:77759722-77759827 | Common:2; Rare:47 | ||||
chr1:77978921-77979296 | Common:3; Rare:140 |