chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1199380295199380296TC4GENIChomozygous108500287
1199380637199380638AG10GENIChomozygous108500291
1199381708199381709AG17GENIChomozygous108500293
1199381956199381957CT11GENIChomozygous120585979
1199383852199383853GC20GENIChomozygous108500301
1199383895199383896TC12GENIChomozygous108500303
1199384143199384144TG16GENIChomozygous108500305
1199384483199384484AT16GENIChomozygous108500307
1199385276199385277TC9GENIChomozygous108500311
1199385884199385885AC8GENIChomozygous108500313
1199386123199386124AG16GENIChomozygous108500315
1199386209199386210TC16GENIChomozygous108500317
1199387689199387690GC5GENIChomozygous120585981
1199387695199387696TG9GENIChomozygous108500321
1199388011199388012GC22GENIChomozygous120585983
1199390203199390204TC21GENIChomozygous108500327
1199391114199391115TA15GENIChomozygous108500329
1199391207199391208AG11GENIChomozygous108500331
1199392185199392186GA23GENIChomozygous108500335
1199392466199392467CT22GENIChomozygous108500339
1199392698199392699TC8GENIChomozygous108500341
1199392845199392846TG9GENIChomozygous108500343
1199393340199393341CT10GENIChomozygous120585985
1199393682199393683CT6GENIChomozygous108500349
1199393901199393902TC13GENIChomozygous108500351
1199395006199395007GA9GENIChomozygous108500357
1199395910199395911GT9GENIChomozygous108500359
1199394513199394514GA4GENICheterozygous125375297