chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71844385518443856GA33GENIChomozygous116116532
71844599518445996GA27GENIChomozygous116116533
71844624618446247TC20GENIChomozygous116116534
71844672618446727CT27GENIChomozygous116116535
71845192518451926AG32GENICpossibly homozygous116116536
71845235918452360GA17GENIChomozygous116116537
71845308118453082GA16GENIChomozygous116116538
71845315718453158CT23GENIChomozygous116116539
71845361518453616GC31GENIChomozygous116116540
71845361618453617TC32GENIChomozygous116116541
71845407518454076CT21GENIChomozygous116116542
71845571318455714CT25GENIChomozygous116116543
71845610618456107TA43GENIChomozygous115587187
71845770118457702CT28GENIChomozygous116116544
71845816318458164AG29GENIChomozygous115587188
71845830918458310TC21GENIChomozygous116116545
71845879218458793CT17GENIChomozygous116116546
71845989318459894AG39GENIChomozygous115587189
71846057018460571TA22GENIChomozygous116116547
71846108918461090AG19GENIChomozygous116116548
71846310218463103AG39GENIChomozygous116116549
71846556218465563GC14GENIChomozygous116116550
71846967818469679AG13GENIChomozygous116116551
71847102318471024CT16GENIChomozygous116116552
71847147618471477AG19GENIChomozygous116116553
71847238318472384AT24GENIChomozygous115587193
71847467118474672TC30GENIChomozygous115587196
71848365018483651GA17GENIChomozygous116116554
71848791818487919TC27GENIChomozygous116116556
71848819818488199GT26GENIChomozygous116116557
71848981418489815AG22GENIChomozygous115587202
71848997818489979TC27GENIChomozygous116116558
71849139318491394AG26GENIChomozygous116116559