Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:70221259-70221682 | Rare:168 | ||||
chr1:70221744-70221950 | Rare:65 | ||||
chr1:70354255-70354502 | Common:1; Rare:86 | ||||
chr1:70354625-70354897 | Common:1; Rare:83 | ||||
chr1:70354992-70355072 | Rare:35 | ||||
chr1:70410632-70410796 | Common:1; Rare:21 | ||||
chr1:70410816-70411406 | Common:4; Rare:140; Clinvar:1; Clinvar (benign):1 | ||||
chr1:71080969-71081416 | Rare:126 | ||||
chr1:72282868-72282977 | Common:3; Rare:47 | ||||
chr1:74198002-74198398 | Common:4; Rare:178 | ||||
chr1:74733002-74733254 | Common:5; Rare:79 | ||||
chr1:74733256-74733321 | Common:1; Rare:31 | ||||
chr1:74733391-74733488 | Rare:41 | ||||
chr1:74733797-74734110 | Common:3; Rare:58 | ||||
chr1:75724248-75724449 | Common:4; Rare:67; Clinvar:2; Clinvar (benign):2 |