chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2263911939263911939G44GENIChomozygous127773735
2263912199263912200CG22GENIChomozygous120351894
2263919590263919590G38GENIChomozygous127773739
2263919610263919610T42GENIChomozygous127773740
2263919628263919629GT42GENIChomozygous110439652
2263919635263919635T38GENIChomozygous127773741
2263919642263919643AT36GENIChomozygous120469921
2263919643263919644TA35GENIChomozygous120469922
2263919653263919654TC34GENIChomozygous110439654
2263921333263921333TC11GENIChomozygous127773743
2263921339263921339T11GENIChomozygous127773744
2263921355263921355C11GENIChomozygous127773745
2263921379263921379T10GENIChomozygous127773746
2263921389263921389T10GENIChomozygous127773747
2263936295263936296AG98GENICheterozygous110439710
2263936304263936304TGT96GENICheterozygous127773751
2263936329263936330GA106GENICheterozygous110439712
2263936472263936473TC101GENICheterozygous110439714
2263936473263936474GA100GENICheterozygous110439716
2263936515263936516T88GENICheterozygous127773752
2263936543263936544CT92GENICheterozygous110439718
2263936583263936584TC72GENICheterozygous110439720
2263936601263936602CT71GENICheterozygous110439722
2263936638263936642ACTC63GENICheterozygous127773753
2263936672263936673TA60GENICpossibly homozygous110439724
2263936704263936705GA57GENICpossibly homozygous110439726