chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
155184457851844579AG44GENIChomozygous112508079
155184489151844892AG30GENIChomozygous112508081
155184713751847138CT40GENIChomozygous112508083
155184841451848415AG18GENIChomozygous112508085
155185325351853254CA28GENICpossibly homozygous112508093
155184839951848400TC21GENIChomozygous113054372
155184940051849401GT20GENIChomozygous112508087
155185023351850234AC41GENIChomozygous112508089
155185323251853233TA27GENIChomozygous112508091
155185439651854397GT28GENIChomozygous112508096
155185644751856448GT42GENIChomozygous112508098
155185650151856502TA43GENIChomozygous112508100