chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
19128823391288234CT26GENIChomozygous108887351
19128926991289270CA34GENIChomozygous108887352
19128983291289833TA24GENIChomozygous108887353
19129030591290306GA33GENIChomozygous108887354
19129106591291066AC22GENIChomozygous108887355
19129110691291107AG23GENIChomozygous108887356
19129168591291686TG27GENIChomozygous108887357
19129192391291924AG19GENIChomozygous108887358
19129236091292361CT21GENIChomozygous108887359
19129237591292376AG20GENIChomozygous108887360
19129251291292513TA22GENIChomozygous108887361
19129251391292514TA22GENIChomozygous108887362
19129264391292644GA27GENIChomozygous108887363
19129287991292880CT27GENIChomozygous108887364
19129355791293558GT19GENIChomozygous108887365
19129368191293682AG18GENIChomozygous108887366
19129405591294056AG33GENIChomozygous108887367
19129528291295283GA28GENIChomozygous108887368
19129528991295290AT25GENIChomozygous108887369
19129547891295479GA14GENIChomozygous108887370
19129568691295687TA25GENIChomozygous108887371
19129569991295700GA22GENIChomozygous108887372
19129616891296169TG3GENIChomozygous108887373
19129684291296843TC3GENIChomozygous108887374
19129715891297159GA17GENIChomozygous108887375
19129716591297166GA14GENIChomozygous108887376
19129745091297451GA27GENIChomozygous108887377