Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:66925207-66925503 | Common:2; Rare:94 | ||||
chr1:66929909-66930405 | Common:1; Rare:151 | ||||
chr1:67429989-67430467 | Rare:181 | ||||
chr1:67833335-67833510 | Common:2; Rare:70 | ||||
chr1:70205542-70205764 | Rare:72 | ||||
chr1:70354659-70354862 | Rare:67 | ||||
chr1:70410627-70410922 | Common:2; Rare:47 | ||||
chr1:70411094-70411303 | Common:1; Rare:50; Clinvar:1; Clinvar (benign):1 | ||||
chr1:71080942-71081379 | Rare:114 | ||||
chr1:72282680-72282973 | Common:4; Rare:88 | ||||
chr1:74198148-74198338 | Common:2; Rare:108 | ||||
chr1:74732968-74733313 | Common:6; Rare:117 | ||||
chr1:75724328-75724427 | Common:3; Rare:33; Clinvar:1; Clinvar (benign):2 | ||||
chr1:76074622-76074856 | Rare:66 | ||||
chr1:77219389-77219498 | Rare:50 |