chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1241503216241503217TC29GENIChomozygous120686215
1241504916241504917AG24GENIChomozygous109541708
1241508294241508295GA16GENIChomozygous120686217
1241510348241510349TA20GENIChomozygous109541720
1241510597241510598CA27GENIChomozygous109541722
1241510618241510619AG28GENIChomozygous120686219
1241510714241510715TC21GENIChomozygous109541724
1241512883241512884CA18GENICheterozygous120686221
1241513737241513738CG23GENIChomozygous109541730
1241514148241514149GA17GENIChomozygous120686223
1241518869241518870AG13GENIChomozygous120686225
1241518908241518909CT20GENIChomozygous120686227
1241518909241518910AG19GENIChomozygous120686229
1241520603241520604CT11GENIChomozygous109541737
1241521061241521062CT13GENIChomozygous109541738
1241522056241522057CG31GENIChomozygous109541742
1241522415241522416TG23GENIChomozygous109541743
1241523644241523645CA28GENIChomozygous109541745
1241525173241525174AG19GENIChomozygous109541747
1241526476241526477TC26GENIChomozygous109541749
1241529892241529893CG19GENIChomozygous109541756
1241530147241530148AG26GENIChomozygous109541758
1241538494241538495GA32GENIChomozygous108591068
1241551846241551847GA21GENIChomozygous109541767
1241553040241553041CT11GENIChomozygous109541768
1241553123241553124TG12GENIChomozygous109541770
1241554677241554678AG31GENIChomozygous109541771
1241555383241555384GT25GENIChomozygous120686231
1241555765241555766TG20GENIChomozygous109541773
1241556074241556075GA26GENIChomozygous109541775
1241556554241556555AT6GENIChomozygous109541778
1241557422241557423AG18GENIChomozygous109541779