Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:70205484-70205770 | Rare:107 | ||||
chr1:70221285-70221540 | Rare:111 | ||||
chr1:70354674-70354883 | Rare:66 | ||||
chr1:70411059-70411357 | Common:2; Rare:78; Clinvar:1; Clinvar (benign):1 | ||||
chr1:71080937-71081400 | Rare:126 | ||||
chr1:74198067-74198338 | Common:3; Rare:138 | ||||
chr1:74733001-74733273 | Common:5; Rare:87 | ||||
chr1:75724284-75724435 | Common:3; Rare:50; Clinvar:1; Clinvar (benign):2 | ||||
chr1:75724622-75724785 | Common:2; Rare:78; Clinvar:4; Clinvar (benign):2 | ||||
chr1:76074566-76074767 | Common:2; Rare:75 | ||||
chr1:77219400-77219552 | Rare:65 | ||||
chr1:77682621-77682716 | Rare:26 | ||||
chr1:77683309-77683572 | Common:1; Rare:86 | ||||
chr1:77779536-77779686 | Rare:50 | ||||
chr1:77978909-77979350 | Common:5; Rare:157 |