chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18238834482388345AG30GENIChomozygous61449386
18238837382388374CT31GENIChomozygous61449387
18238878482388785TC19GENIChomozygous61449388
18238881282388813AG15GENIChomozygous61449389
18238911982389120TA36GENIChomozygous61449390
18238961882389619TC20GENIChomozygous61449391
18238964882389649CG23GENIChomozygous61449392
18238973082389731TC34GENIChomozygous62084904
18238973282389733AT33GENIChomozygous62084905
18239014982390150GT16GENIChomozygous61449393
18239020782390209TG--1GENIChomozygous61449394
18239023082390231TTGTG7GENIChomozygous62259857
18239056082390561AG29GENIChomozygous61449399
18239069082390691AG30GENIChomozygous61449401
18239081682390817TC32GENIChomozygous61449402
18239103782391038AAGG24GENIChomozygous61883954
18239146182391462CG23GENIChomozygous62687220
18239148482391485GT27GENIChomozygous62084906
18239163682391637TC24GENIChomozygous61449404
18239174382391744A-22GENIChomozygous61449406
18239196982391970GC12GENIChomozygous61449407
18239256782392568CA15GENIChomozygous62687221
18239271582392716AG26GENIChomozygous61449408
18239311382393120TTTTTTT-------9GENICheterozygous61669416
18239311482393120TTTTTT------9GENICheterozygous62137305
18239376882393769AC7GENIChomozygous61449410
18239380482393805GT11GENIChomozygous61883956
18239395482393955TC20GENIChomozygous61449411