chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
147390645273906453GGT10GENIChomozygous48790582
147390648073906481T-8GENIChomozygous48790584
147390650973906510T-12GENIChomozygous48790585
147390653073906531GGT15GENIChomozygous48790586
147390654873906549T-15GENIChomozygous48790587
147390656473906565T-15GENIChomozygous48790588
147391024173910242G-20GENIChomozygous48790597
147391704173917042AG33GENIChomozygous48790604
147391731773917318CT21GENICheterozygous48790605
147391733873917339GGTTATAAAA20GENICheterozygous48790606
147391739973917403TATT----8GENICheterozygous48790607
147391740873917409AATTTATTTT9GENICheterozygous49326871
147392644673926447TTA11GENIChomozygous48790624
147392677573926777AA--21GENIChomozygous49314553
147392677873926779TTGC22GENIChomozygous49314554
147392972773929731TTCT----3GENIChomozygous49340280
147392041373920414G-10GENIChomozygous49340278
147392146073921461AAT14GENICheterozygous49340279
147393259373932594TA6GENIChomozygous48790632
147393261573932616TTA2GENIChomozygous48790633
147394250373942507GAAA----21GENIChomozygous48790640
147395983473959835CCTT8GENICheterozygous48790667
147395983573959836T-8GENICheterozygous48790668
147396681273966813GGT17GENIChomozygous48790672
147396684473966845AAT19GENIChomozygous48790673
147396686473966865GGA17GENIChomozygous48790674
147396688173966882GGT21GENIChomozygous48790675
147396688373966884AAT22GENIChomozygous48790676
147396688873966889CCT23GENIChomozygous48790677
147396689473966895A-24GENIChomozygous48790678
147396694973966950CA18GENIChomozygous48790679