chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
201088708510887086TC29GENIChomozygous109091586
201088782510887826AC20GENIChomozygous109091588
201089077410890775CT28GENIChomozygous109238408
201089122110891222CA19GENIChomozygous109238409
201089251010892511GA16GENIChomozygous109507564
201089541310895414TA27GENIChomozygous109507566
201089716810897169TC12GENIChomozygous109238410
201089721510897216TC16GENIChomozygous109091594
201089722410897225CT13GENIChomozygous109507568
201089730310897304TC16GENIChomozygous109091596
201089760210897603GC22GENIChomozygous109507570
201089768810897689TA21GENIChomozygous109091598
201089835410898355AT13GENIChomozygous109507572
201089835510898356AT13GENIChomozygous109507574
201089835610898357AT13GENIChomozygous109507576
201090099010900991CT25GENIChomozygous109422519
201090168810901689TC10GENIChomozygous109422523
201090184710901848AC5GENIChomozygous109572680
201090184810901849TA5GENIChomozygous109572681
201090259810902599CA22GENIChomozygous109507578
201090547810905479TC25GENIChomozygous109507580
201090702010907021CT16GENIChomozygous109091610
201090858410908585CT9GENIChomozygous109507582
201090950210909503CT11GENIChomozygous109238414
201090976210909763TG23GENIChomozygous109091618
201090976610909767TC23GENIChomozygous109091620
201091060410910605CT17GENIChomozygous109091622
201091068410910685GA18GENIChomozygous109091624
201091158510911586GC18GENIChomozygous109507584