Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:169367780-169367962 | Common:2; Rare:30 | ||||
chr1:169794897-169795110 | Common:3; Rare:58 | ||||
chr1:170074683-170074762 | Common:1; Rare:21 | ||||
chr1:170532040-170532178 | Rare:60; Clinvar:1 | ||||
chr1:171741929-171742151 | Common:1; Rare:74 | ||||
chr1:171781383-171781737 | Common:4; Rare:93 | ||||
chr1:173477008-173477434 | Common:5; Rare:146 | ||||
chr1:173824348-173824708 | Rare:68; Clinvar:1 | ||||
chr1:173867979-173868383 | Common:2; Rare:133 | ||||
chr1:174159352-174159549 | Common:2; Rare:76 | ||||
chr1:174999328-174999493 | Common:1; Rare:43 | ||||
chr1:174999644-175000114 | Common:1; Rare:138 | ||||
chr1:178725098-178725298 | Common:10; Rare:81 | ||||
chr1:179882493-179882841 | Rare:167; Clinvar:7; Clinvar (benign):2 | ||||
chr1:182604381-182604509 | Rare:27 |