chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1274311929274311930GA37GENIChomozygous108654365
1274316490274316491CA26GENICpossibly homozygous108654367
1274316692274316693CA48GENIChomozygous108654369
1274316816274316817GA68GENIChomozygous108654371
1274316914274316915GA57GENICpossibly homozygous108654372
1274317197274317198AG29GENIChomozygous108654374
1274320892274320893CT35GENIChomozygous108654375
1274321725274321726GT38GENICpossibly homozygous108654377
1274325325274325326TC49GENIChomozygous108654379
1274325645274325646TA29GENICheterozygous108654380
1274326566274326567TG12GENIChomozygous108654382
1274327584274327585GC21GENIChomozygous108654384
1274330279274330280CG44GENIChomozygous108654386
1274331163274331164AG44GENIChomozygous108654387
1274331791274331792AG18GENIChomozygous108654389
1274334571274334572TC9GENIChomozygous108654391
1274334970274334971CT48GENIChomozygous108654392
1274335215274335216GA27GENIChomozygous108654394
1274336802274336803CT55GENIChomozygous108654396
1274344226274344227AG41GENIChomozygous108654398
1274349690274349691TC98GENICheterozygous108654400
1274349836274349837AG74GENICheterozygous108654402
1274350086274350087TC63GENICheterozygous108654403
1274350144274350145GA68GENICheterozygous108654405
1274350149274350150CT71GENICheterozygous108654407
1274351836274351837CT65GENICheterozygous108654409
1274352443274352444GA106GENICheterozygous108654411
1274352744274352745CA36GENICheterozygous108654413