chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
62289281922892819GT10GENICheterozygous137674605
62300393923003940CA35GENICheterozygous154348179
62300396523003966CT32GENICheterozygous154348180
62305613123056133AC28GENICheterozygous143974441
62310592623105927GC4GENIChomozygous137743786
62311536223115363TC33GENICheterozygous137743788
62311786623117869CTC33GENICheterozygous140887656
62315622723156228GA9GENIChomozygous137743790
62315826623158267GA11GENIChomozygous403168326
62315826623158267G11GENICheterozygous403168327
62319556223195563T8GENICheterozygous403168328
62319556223195563TG8GENICheterozygous403168329
62319556223195563TA8GENICheterozygous403168330
62319556523195566G16GENICheterozygous403168331
62319556523195566GT16GENIChomozygous403168332
62319557123195572C16GENICheterozygous403168333
62319557123195572CA16GENICheterozygous403168334
62319557123195572CT16GENIChomozygous403168335
62319557323195574A10GENICheterozygous403769533
62319850223198503T16GENIChomozygous137674682
62331081823310820CT29GENIChomozygous137674716
62336072623360728TC15GENICheterozygous141091612
62317477323174774GA20GENIChomozygous148514293
62319557323195574AT10GENICheterozygous403769534
62333273123332732GA10GENIChomozygous403168340
62333273123332732G10GENICheterozygous403168341
62328675023286752TC9GENICheterozygous148509155
62344629123446292GA18GENICheterozygous154359134
62344629123446292G18GENICheterozygous403168343
62345866123458663AC23GENICheterozygous141116662
62347011023470111GA26GENICheterozygous148514294
62349384823493849GC11GENIChomozygous137744219
62352618923526190TC15GENIChomozygous137744298
62354220223542203G13GENICheterozygous403168346
62354220223542203GA13GENICheterozygous403168347
62355968423559685T13GENICheterozygous403168348
62355968423559685TA13GENICheterozygous403168349
62357088323570884TA12GENICheterozygous154361551
62357088323570884T12GENICheterozygous403168350
62357741523577416TC23GENIChomozygous137744398
62359188023591881A12GENIChomozygous403168352
62359188023591881AG12GENICheterozygous403168353