chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4208769186208769187CT14GENIChomozygous58601484
4208769488208769489A-13GENIChomozygous58601486
4208769525208769526CT13GENIChomozygous58601488
4208769664208769665TC11GENICpossibly homozygous57066957
4208770232208770233A-20GENIChomozygous57066958
4208771598208771599CT26GENIChomozygous58601490
4208775145208775146AG18GENIChomozygous57607916
4208774071208774072GT18GENIChomozygous57607910
4208774448208774449TC17GENIChomozygous57607912
4208777453208777454GA27GENIChomozygous58601492
4208777824208777825TC24GENIChomozygous57066962
4208778918208778919AG27GENIChomozygous58601494
4208779028208779029CT21GENIChomozygous57066963
4208779043208779044CG17GENIChomozygous57066964
4208779675208779676TA16GENIChomozygous58601496
4208779777208779779AC--12GENIChomozygous58601498
4208780143208780144CT15GENIChomozygous58601500
4208780593208780594CCAT4GENICheterozygous58531211
4208780595208780596CCATACATACACAG14GENIChomozygous58601502
4208780682208780683AAT15GENIChomozygous57066967
4208782787208782788TC22GENIChomozygous58601504
4208782951208782952CT19GENIChomozygous57066969
4208783383208783384CG19GENIChomozygous57607930
4208783620208783621GT23GENIChomozygous57066972
4208784079208784080GC28GENIChomozygous57066973