chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5149556201149556202CT16GENIChomozygous137649492
5149559255149559256AT30GENIChomozygous137649493
5149560678149560679CA24GENIChomozygous137649494
5149561425149561426TC27GENIChomozygous137649495
5149564779149564780AG28GENIChomozygous137649496
5149569241149569242AG10GENIChomozygous137649497
5149570758149570759AT30GENIChomozygous137649498
5149572049149572050GA17GENIChomozygous137649499
5149572645149572648TCT24GENIChomozygous137348723
5149566060149566061A24GENIChomozygous137348721
5149569014149569019AAGAT21GENIChomozygous137348722
5149572720149572721GA22GENIChomozygous137649500
5149573611149573612AG23GENIChomozygous137649501
5149574150149574151CT22GENIChomozygous137649502
5149574352149574353CT23GENIChomozygous137649503
5149574825149574825CACA23GENIChomozygous137348724
5149575471149575472TC28GENIChomozygous137649504
5149576918149576919TC18GENIChomozygous137649505
5149577372149577373GA35GENIChomozygous137649506
5149578824149578824AC22GENIChomozygous137348725
5149578826149578826CTGGGAAAGATG24GENIChomozygous137348726
5149581132149581132AGGC23GENICpossibly homozygous137348727
5149581330149581331CT24GENIChomozygous137649507
5149581989149581990TC36GENIChomozygous137649508
5149582257149582258AG25GENIChomozygous137649509
5149582688149582689AC24GENIChomozygous137649510
5149582900149582901GC16GENIChomozygous137649511
5149584771149584772GA31GENIChomozygous137649512
5149586467149586467T25GENIChomozygous137348728
5149586999149586999T31GENIChomozygous137348729
5149587901149587902GA17GENIChomozygous137649513
5149588047149588048AG31GENIChomozygous137649514
5149588142149588142AC37GENIChomozygous137348730
5149589015149589016AG26GENIChomozygous137649515
5149589321149589322GT33GENIChomozygous137649516
5149590312149590312A30GENICpossibly homozygous137348731
5149592125149592125A21GENIChomozygous137348732
5149592137149592138AC20GENIChomozygous137649517
5149592454149592455TC33GENIChomozygous137649518