chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
156051529760515298A-19GENICheterozygous697967656
156051838060518381GA16GENIChomozygous540625995
156052210260522103TA4GENICheterozygous540625996
156052716460527165GA18GENICheterozygous540625997
156053714560537146AAG14GENIChomozygous697967657
156053751060537511CCG31GENIChomozygous697967658
156054125360541255GG--11GENICheterozygous697967659
156054125660541257CT17GENICheterozygous540625998
156056387360563874A-8GENIChomozygous697967660
156056388160563882AAT6GENIChomozygous697967661
156056389960563900GT15GENIChomozygous540625999
156056390060563901GT15GENIChomozygous540626000
156056486760564868AG21GENIChomozygous538022742
156057458760574588TC25GENICpossibly homozygous540626001
156059271560592716TTTCTA7GENICpossibly homozygous697967662
156063699860636999AG36GENIChomozygous538022743
156065834060658341A-8GENICheterozygous697967663
156068638560686386TG15GENIChomozygous540626002