chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121105463811054639TC16GENIChomozygous126167373
121105505811055059AC22GENIChomozygous126167374
121105538511055386AG24GENIChomozygous126167375
121105613411056135CT29GENIChomozygous118322115
121105627911056280GC5GENICheterozygous126223348
121105937611059377AG17GENIChomozygous126167376
121106146211061463AG18GENIChomozygous126167377
121106152711061528AC16GENIChomozygous126167378
121106207211062073TG26GENIChomozygous126167379
121106211311062114AG10GENIChomozygous126167380
121106213511062136GC12GENIChomozygous126167381
121106291711062918GA17GENIChomozygous126167382
121106295711062958AG21GENIChomozygous126167383
121106315111063152GA21GENIChomozygous126167384
121106323811063239CG28GENIChomozygous126167385
121106356911063570TC21GENIChomozygous126167386
121106376911063770AT17GENIChomozygous126167387
121106393311063934AG27GENIChomozygous126167388
121106480211064803AG19GENICpossibly homozygous126167389
121106487811064879TG15GENIChomozygous126167390
121106516111065162TG16GENIChomozygous126167391
121106564011065641TG14GENIChomozygous126167392
121106655711066558CT16GENIChomozygous126167393
121106669011066691TC9GENIChomozygous126167394
121106718511067186CT8GENIChomozygous126167396
121106767411067675CT3GENICheterozygous126223349
121106768611067687CT6GENIChomozygous126223350
121106841011068411GT22GENICheterozygous126167397
121107040111070402AG23GENIChomozygous126167398
121107085611070857AG18GENIChomozygous126167399
121107092011070921AT14GENIChomozygous126167400
121107100111071002CT27GENIChomozygous126167401
121107125711071258TG22GENIChomozygous126167402
121107125811071259TG22GENIChomozygous126167403
121107130411071305TG17GENICpossibly homozygous126167404
121107219311072194AG15GENIChomozygous126167405
121107281611072817TC21GENIChomozygous126167406
121107863811078639AG4GENICheterozygous126223351
121107969311079694AC5GENIChomozygous126167409
121108231411082315GA29GENIChomozygous126167411