chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71844385518443856GA25GENIChomozygous116116532
71844546918445470CG25GENIChomozygous115587183
71844599518445996GA21GENIChomozygous116116533
71844624618446247TC17GENIChomozygous116116534
71844672618446727CT33GENIChomozygous116116535
71845192518451926AG33GENIChomozygous116116536
71845235918452360GA24GENIChomozygous116116537
71845308118453082GA24GENIChomozygous116116538
71845315718453158CT23GENIChomozygous116116539
71845361518453616GC27GENIChomozygous116116540
71845361618453617TC27GENIChomozygous116116541
71845407518454076CT22GENIChomozygous116116542
71845571318455714CT17GENIChomozygous116116543
71845610618456107TA27GENIChomozygous115587187
71845770118457702CT31GENIChomozygous116116544
71845816318458164AG20GENIChomozygous115587188
71845830918458310TC19GENIChomozygous116116545
71845879218458793CT22GENIChomozygous116116546
71845989318459894AG29GENIChomozygous115587189
71846057018460571TA19GENIChomozygous116116547
71846108918461090AG17GENIChomozygous116116548
71846310218463103AG30GENIChomozygous116116549
71846556218465563GC29GENIChomozygous116116550
71846967818469679AG18GENIChomozygous116116551
71847102318471024CT19GENICpossibly homozygous116116552
71847147618471477AG22GENIChomozygous116116553
71847238318472384AT16GENIChomozygous115587193
71847467118474672TC35GENIChomozygous115587196
71848365018483651GA25GENIChomozygous116116554
71848791818487919TC24GENIChomozygous116116556
71848819818488199GT18GENIChomozygous116116557
71848981418489815AG31GENIChomozygous115587202
71848997818489979TC19GENIChomozygous116116558
71849139318491394AG19GENIChomozygous116116559