Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:68232499-68232673 | Rare:38 | ||||
chr1:69567850-69568017 | Common:1; Rare:39 | ||||
chr1:69568101-69568407 | Common:2; Rare:91 | ||||
chr1:69568629-69568806 | Common:1; Rare:62 | ||||
chr1:70205475-70205778 | Rare:109 | ||||
chr1:70221268-70221721 | Rare:186 | ||||
chr1:70354634-70354862 | Rare:75 | ||||
chr1:70411059-70411313 | Common:2; Rare:65; Clinvar:1; Clinvar (benign):1 | ||||
chr1:71080950-71081401 | Rare:125 | ||||
chr1:72282829-72283382 | Common:7; Rare:178 | ||||
chr1:74198141-74198340 | Common:2; Rare:112 | ||||
chr1:74733092-74733259 | Common:3; Rare:46 | ||||
chr1:75134286-75134591 | Common:2; Rare:56 | ||||
chr1:75724277-75724773 | Common:6; Rare:174; Clinvar:7; Clinvar (benign):5 | ||||
chr1:76074572-76074796 | Common:2; Rare:79 |