Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:10398797-10399103 | Common:2; Rare:117 | ||||
chr1:10474870-10474975 | Rare:28; Clinvar:1 | ||||
chr1:11262511-11262828 | Common:1; Rare:93 | ||||
chr1:11654731-11654901 | Common:4; Rare:51 | ||||
chr1:11691473-11691763 | Common:4; Rare:66 | ||||
chr1:11691765-11691840 | Rare:11 | ||||
chr1:11735976-11736186 | Common:3; Rare:62 | ||||
chr1:11805932-11806255 | Common:2; Rare:87; Clinvar:1 | ||||
chr1:11934553-11934743 | Common:3; Rare:61; Clinvar:5 | ||||
chr1:16352400-16352581 | Common:3; Rare:100 | ||||
chr1:16613525-16613645 | |||||
chr1:17053991-17054316 | Common:3; Rare:99; Clinvar:6; Clinvar (benign):8 | ||||
chr1:17439740-17439889 | Rare:57 | ||||
chr1:19210115-19210417 | Rare:108 | ||||
chr1:19251512-19251876 | Common:6; Rare:120 |