chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18238834482388345AG20GENIChomozygous61449386
18238837382388374CT23GENIChomozygous61449387
18238878482388785TC27GENIChomozygous61449388
18238881282388813AG34GENIChomozygous61449389
18238911982389120TA24GENIChomozygous61449390
18238961882389619TC32GENIChomozygous61449391
18238964882389649CG34GENIChomozygous61449392
18238973082389731TC21GENIChomozygous62084904
18238973282389733AT22GENIChomozygous62084905
18239014982390150GT27GENIChomozygous61449393
18239020782390209TG--4GENIChomozygous61449394
18239023082390231TTGTG8GENIChomozygous62259857
18239056082390561AG22GENIChomozygous61449399
18239069082390691AG31GENIChomozygous61449401
18239081682390817TC31GENIChomozygous61449402
18239103782391038AAGG23GENIChomozygous61883954
18239146182391462CG20GENIChomozygous62687220
18239148482391485GT17GENIChomozygous62084906
18239163682391637TC23GENIChomozygous61449404
18239174382391744A-19GENIChomozygous61449406
18239196982391970GC33GENIChomozygous61449407
18239256782392568CA29GENIChomozygous62687221
18239271582392716AG19GENICpossibly homozygous61449408
18239311482393120TTTTTT------8GENIChomozygous62137305
18239376882393769AC26GENIChomozygous61449410
18239380482393805GT33GENIChomozygous61883956
18239395482393955TC31GENIChomozygous61449411