chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7123584109123584110CT35GENIChomozygous638126390
7123584118123584119TC36GENIChomozygous638126391
7123584134123584135CT36GENIChomozygous638126392
7123584139123584140CT38GENICpossibly homozygous638126393
7123584468123584469CT26GENIChomozygous638126394
7123584484123584485GA30GENIChomozygous638126395
7123585204123585205CG32GENIChomozygous638126396
7123585329123585330CT23GENIChomozygous638126397
7123586152123586153TC39GENIChomozygous638126398
7123586597123586598GT29GENIChomozygous638126399
7123586763123586764AG29GENIChomozygous638126400
7123587073123587074CA36GENIChomozygous638126401
7123587605123587621TTCATTCATTCAGTGT----------------4GENIChomozygous749797478
7123589080123589081AG40GENIChomozygous638126402
7123589463123589464CT35GENIChomozygous638126403
7123589994123590002ACACACAT--------10GENICheterozygous749797479
7123592069123592077CCTTCCTT--------3GENIChomozygous749797482