chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1170262372170262373AC21GENIChomozygous108375500
1170262418170262419AC21GENIChomozygous108375502
1170262757170262758AG21GENIChomozygous108375504
1170262979170262980CT25GENIChomozygous108375506
1170263862170263863AG23GENIChomozygous108375508
1170264182170264183TC16GENIChomozygous108375510
1170264224170264225AG18GENIChomozygous108375512
1170264473170264474AG25GENIChomozygous108375514
1170264622170264623AG17GENIChomozygous108375516
1170265005170265006GA16GENIChomozygous108375518
1170265015170265016AG15GENIChomozygous108375520
1170265119170265120T21GENIChomozygous127455468
1170265193170265198GACTA19GENIChomozygous127455469
1170265503170265504TC28GENIChomozygous108375522
1170265683170265684TC13GENIChomozygous108375524
1170266684170266686CA8GENIChomozygous127455470
1170266750170266751CT8GENIChomozygous108375526
1170266986170266987CT12GENIChomozygous108375528
1170267002170267003GA11GENIChomozygous108375530
1170267220170267221CT9GENIChomozygous108375532
1170267885170267886GA24GENIChomozygous108375536
1170267919170267920AG26GENIChomozygous108375538
1170269227170269228TC21GENIChomozygous108375540
1170269278170269279TG18GENIChomozygous108375542
1170269659170269660GA15GENIChomozygous108375544
1170270944170270945TC23GENIChomozygous108375546
1170271310170271311CG27GENIChomozygous108375548
1170271689170271690AG14GENIChomozygous108375550
1170272010170272011GA8GENIChomozygous108375552