chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5149556201149556202CT35GENIChomozygous137649492
5149559255149559256AT53GENIChomozygous137649493
5149560678149560679CA41GENIChomozygous137649494
5149561425149561426TC42GENIChomozygous137649495
5149564779149564780AG47GENIChomozygous137649496
5149566060149566061A34GENIChomozygous137348721
5149569014149569019AAGAT50GENIChomozygous137348722
5149569241149569242AG12GENIChomozygous137649497
5149570758149570759AT39GENIChomozygous137649498
5149572049149572050GA38GENIChomozygous137649499
5149572645149572648TCT49GENIChomozygous137348723
5149572720149572721GA49GENIChomozygous137649500
5149573611149573612AG55GENIChomozygous137649501
5149574150149574151CT39GENIChomozygous137649502
5149574352149574353CT41GENIChomozygous137649503
5149574825149574825CACA29GENIChomozygous137348724
5149575471149575472TC33GENIChomozygous137649504
5149576918149576919TC61GENIChomozygous137649505
5149577372149577373GA43GENIChomozygous137649506
5149578824149578824AC56GENIChomozygous137348725
5149578826149578826CTGGGAAAGATG56GENIChomozygous137348726
5149581132149581132AGGC40GENIChomozygous137348727
5149581330149581331CT52GENIChomozygous137649507
5149581989149581990TC55GENIChomozygous137649508
5149582257149582258AG49GENIChomozygous137649509
5149582688149582689AC48GENIChomozygous137649510
5149582900149582901GC41GENIChomozygous137649511
5149584771149584772GA44GENIChomozygous137649512
5149586467149586467T61GENIChomozygous137348728
5149586999149586999T59GENIChomozygous137348729
5149587901149587902GA47GENIChomozygous137649513
5149588047149588048AG53GENIChomozygous137649514
5149588142149588142AC58GENIChomozygous137348730
5149589015149589016AG60GENIChomozygous137649515
5149589321149589322GT55GENIChomozygous137649516
5149590312149590312A61GENICpossibly homozygous137348731
5149592125149592125A45GENIChomozygous137348732
5149592137149592138AC49GENIChomozygous137649517
5149592454149592455TC47GENIChomozygous137649518