chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
162029811020298111AG60GENICpossibly homozygous111752476
162029931620299317CT78GENIChomozygous111752478
162029991420299915AG60GENIChomozygous111752480
162030081920300820GC55GENIChomozygous111752482
162030105020301051AG73GENIChomozygous111752484
162030123420301235TA58GENIChomozygous111752486
162030160620301607AG45GENIChomozygous111752488
162030166620301667CT28GENIChomozygous111752490
162030185320301854AG67GENICpossibly homozygous111752492
162030256420302565TC35GENIChomozygous111752494
162030352820303529AG87GENIChomozygous111752496
162030369820303699AG54GENIChomozygous111752498
162030396120303962TC43GENICpossibly homozygous112130273
162030403620304037AG54GENIChomozygous111752500
162030416320304164TC34GENIChomozygous111752502
162030530520305306TA45GENIChomozygous111752504
162030650020306501TC52GENIChomozygous111752506
162030685220306853CG43GENIChomozygous111752508
162030704220307043GA49GENIChomozygous111752510
162030722720307228GA57GENICpossibly homozygous111752512