Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:67053619-67053776 | Common:4; Rare:62 | ||||
chr1:67429993-67430439 | Rare:171 | ||||
chr1:67833342-67833527 | Common:2; Rare:73 | ||||
chr1:68232462-68232633 | Rare:39 | ||||
chr1:70205509-70205778 | Rare:96 | ||||
chr1:70354680-70354842 | Rare:59 | ||||
chr1:70411053-70411268 | Common:1; Rare:52; Clinvar:1 | ||||
chr1:71080938-71081354 | Rare:113 | ||||
chr1:72282669-72282976 | Common:4; Rare:91 | ||||
chr1:74198152-74198324 | Common:1; Rare:101 | ||||
chr1:74732994-74733334 | Common:6; Rare:120 | ||||
chr1:76074629-76074851 | Rare:62 | ||||
chr1:77219400-77219476 | Rare:38 | ||||
chr1:77683348-77683548 | Common:1; Rare:66 | ||||
chr1:77888351-77888758 | Common:2; Rare:92; Clinvar:2; Clinvar (benign):1 |