Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:63593323-63593503 | Rare:69; Clinvar (benign):1 | ||||
chr1:64841281-64841529 | Rare:55; Clinvar:1 | ||||
chr1:66924820-66925024 | Rare:89 | ||||
chr1:66925182-66925514 | Common:2; Rare:106 | ||||
chr1:67053643-67053776 | Common:4; Rare:55 | ||||
chr1:67053941-67054175 | Common:1; Rare:85 | ||||
chr1:67429989-67430279 | Rare:98 | ||||
chr1:67833342-67833520 | Common:2; Rare:72 | ||||
chr1:70205542-70205770 | Rare:72 | ||||
chr1:70221306-70221506 | Rare:85 | ||||
chr1:70354697-70354838 | Rare:51 | ||||
chr1:71080945-71081383 | Rare:117 | ||||
chr1:72282812-72282961 | Common:3; Rare:48 | ||||
chr1:74198148-74198320 | Common:1; Rare:99 | ||||
chr1:74732994-74733259 | Common:5; Rare:82 |