chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
192970111029701111GT13GENIChomozygous46238464
192970134129701342CT25GENIChomozygous46238465
192970139629701397TC27GENIChomozygous46238466
192970140229701403TC28GENIChomozygous46238467
192970156229701563CG23GENIChomozygous46238468
192970164929701650AG30GENIChomozygous46238469
192970184629701847GT29GENIChomozygous46238470
192970185329701854TTCCGTA26GENIChomozygous46238471
192970263829702639AC32GENIChomozygous46238473
192970293329702934GA32GENIChomozygous46238474
192970319529703196AC36GENIChomozygous46238475
192970332129703322GT25GENIChomozygous46238476
192970217929702180CCATGTGTGT19GENICheterozygous46429256
192970217929702180CCATGTGAGT19GENICpossibly homozygous46677316