chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
47869508178695082AT18GENIChomozygous113125879
47869540178695402CT10GENIChomozygous113459139
47869628078696281TC22GENIChomozygous113125880
47869688578696886GT25GENIChomozygous113125882
47869699078696991GC19GENIChomozygous113125883
47869726378697264TC26GENIChomozygous113125884
47869787678697877AG11GENIChomozygous113125885
47869803778698038GA20GENIChomozygous113459141
47869897278698973TC16GENIChomozygous113125887
47870381578703816AC25GENIChomozygous113125892
47870389878703899AG24GENIChomozygous113125894
47870702178707022GA23GENIChomozygous113125896
47870717678707177CG22GENIChomozygous113125897
47870735978707360CT20GENIChomozygous113125899
47870759078707591GA18GENIChomozygous113125900
47870759178707592CA18GENIChomozygous113125901
47870766478707665CA11GENIChomozygous113459143
47870811578708116GA9GENIChomozygous113125902
47870819578708196TC18GENIChomozygous113125903
47870854678708547GA18GENIChomozygous113459145
47870901578709016AG18GENIChomozygous113125904
47870910778709108AG25GENIChomozygous113125905
47870922878709229AC26GENIChomozygous113125906
47870969678709697TC22GENIChomozygous113125907
47871022078710221CT17GENIChomozygous113125908
47871034678710347GA25GENIChomozygous113125909
47871060878710609CA22GENIChomozygous113459147
47871088278710883CT27GENIChomozygous113125911
47871122878711229GA19GENIChomozygous113459149
47871233478712335GA18GENIChomozygous113459151
47871288478712885GA23GENIChomozygous113459153
47871489678714897TC11GENIChomozygous113459155
47871538778715388AG29GENIChomozygous113125915
47871560278715603AG16GENIChomozygous113125916