chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4157359635157359636AT14GENIChomozygous112906001
4157359881157359882GT18GENIChomozygous112906003
4157359944157359945GA19GENIChomozygous112906005
4157360418157360419AG33GENIChomozygous112906007
4157360747157360748GC17GENIChomozygous112906009
4157362577157362578TC19GENIChomozygous112906013
4157363021157363022GA17GENIChomozygous112906015
4157363067157363068AT15GENIChomozygous112906017
4157363425157363426AG15GENIChomozygous112906019
4157364093157364094GC18GENIChomozygous112906021
4157366179157366180CT16GENIChomozygous112906025
4157366408157366409TC10GENIChomozygous112906027
4157368042157368043GA18GENICpossibly homozygous112906029
4157368053157368054GA18GENIChomozygous112906031
4157371222157371223CT16GENIChomozygous112906033
4157371533157371534CA14GENIChomozygous112906035
4157372117157372118GA16GENICpossibly homozygous112906037
4157372818157372819AG8GENIChomozygous112906039
4157374616157374617AG3GENIChomozygous112906041
4157374714157374715CG8GENIChomozygous112906043