chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
134851310848513109CT39GENIChomozygous114549313
134851376748513768TA36GENIChomozygous114549314
134851448248514483AC34GENICpossibly homozygous114549315
134851457748514578TC24GENIChomozygous114549316
134852563948525640GC14GENIChomozygous114549317
134852590448525905GA39GENIChomozygous114549318
134852826448528265CT36GENIChomozygous114549319
134852887348528874CT39GENIChomozygous114615751
134852999448529995CA26GENIChomozygous114549320
134853179648531797GA40GENIChomozygous114549321
134853197948531980GA42GENIChomozygous114549322
134853213548532136CT38GENIChomozygous114549323
134853224848532249TC35GENIChomozygous114615752
134853320748533208TG27GENIChomozygous114549324
134853322048533221AG31GENIChomozygous114549325
134853393348533934GA46GENIChomozygous114549326
134853643848536439GA24GENIChomozygous114549328
134853757548537576GA44GENIChomozygous114549329
134853769048537691CA21GENIChomozygous114615753
134853795348537954TC21GENIChomozygous114549330
134853795448537955TC21GENIChomozygous114549331
134853826548538266CG29GENIChomozygous114549332
134853859148538592GC24GENIChomozygous114549333
134853923848539239CT23GENIChomozygous114549334