chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8115512383115512384CT27GENICheterozygous926609749
8115513030115513031CT8GENICheterozygous926609750
8115516330115516331CCG86GENICheterozygous926646774
8115518076115518077AG29GENICheterozygous926609751
8115519250115519251GA15GENICheterozygous926609752
8115523834115523835AG55GENICheterozygous926609753
8115527949115527950AC12GENICheterozygous926609754
8115527950115527951GA11GENICheterozygous926609755
8115541589115541590AAG17GENICheterozygous926646775
8115555931115555932CT45GENICheterozygous926609756
8115583690115583691CT21GENICheterozygous926609757
8115583713115583714C-20GENICheterozygous926646776
8115587025115587026CT30GENICheterozygous926609758
8115592854115592855AG16GENICheterozygous926609759
8115616477115616478AG22GENICheterozygous926609760
8115622529115622531CT--15GENICheterozygous926646777
8115626308115626309AT17GENICheterozygous926609761
8115632953115632954CT38GENICheterozygous926609762
8115639625115639626TA10GENICheterozygous926609763