chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
46760719767607198CT45GENIChomozygous112689254
46760735667607357CT67GENIChomozygous112689256
46760793867607939AG63GENIChomozygous112689258
46760795167607952AT64GENIChomozygous112689260
46760828267608283GC61GENIChomozygous112689262
46760894767608948CA22GENICheterozygous112689264
46760907467609075TG67GENICpossibly homozygous112689266
46760915467609155AC63GENIChomozygous112689268
46761015867610159GA48GENICpossibly homozygous112689270
46761017167610172AG51GENICpossibly homozygous112689272
46761189467611895AT49GENIChomozygous112689274
46761212467612125TA82GENIChomozygous112689276
46761392767613928AC79GENIChomozygous112689278
46761474867614749CT62GENIChomozygous112689280
46761505367615054GA55GENICpossibly homozygous112689282
46761507967615080AT54GENIChomozygous112689284
46761509067615091TC57GENIChomozygous112689287
46761592667615927AT42GENIChomozygous112689289