chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71105517111055172GA18GENIChomozygous115567901
71105612411056125CA26GENIChomozygous115567902
71105696611056967AG23GENIChomozygous115567903
71105893611058937AT20GENIChomozygous115567907
71105984711059848GC24GENIChomozygous115567908
71106024511060246TC16GENICpossibly homozygous115567910
71106028911060290GA19GENIChomozygous115567911
71106029011060291CA19GENIChomozygous115567912
71106037111060372CA18GENIChomozygous115567913
71106103611061037AG31GENIChomozygous115567914
71106107211061073GA29GENIChomozygous115567915
71106123211061233GT15GENIChomozygous115567916
71106132411061325AG26GENIChomozygous115567917
71106918611069187CT30GENIChomozygous115567918
71107196711071968TG12GENIChomozygous115567919
71107202011072021GT6GENICheterozygous118391186
71107202111072022AT6GENICheterozygous118391187
71107202211072023AT6GENICheterozygous118391188
71107263211072633TG24GENIChomozygous115567924
71107426111074262AG24GENIChomozygous115567925
71107494911074950TA17GENIChomozygous115567926
71107510811075109GA29GENIChomozygous115567927