chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141410852314108524AG14GENIChomozygous113907746
141410866014108661CT22GENIChomozygous113907748
141410866414108665TC22GENIChomozygous113907750
141410873414108735TC18GENIChomozygous113907752
141410884814108849TC18GENIChomozygous113907754
141410893314108934CT22GENIChomozygous113907756
141410962614109627AG23GENIChomozygous113907758
141411002314110024GA18GENIChomozygous113907760
141411005514110056AG22GENIChomozygous113907762
141411069014110691CA10GENIChomozygous113926127
141411130214111303GA33GENIChomozygous113907764
141411209714112098GA19GENIChomozygous113907766
141411276714112768TC24GENICpossibly homozygous113907768
141411430214114303AG26GENIChomozygous113351465
141411530314115304CA21GENIChomozygous113907772
141411933914119340AG27GENIChomozygous113659173
141411949114119492CT14GENIChomozygous113907774
141412075014120751CT26GENICpossibly homozygous113351479
141412098514120986AG28GENIChomozygous113907776
141412103814121039CT24GENIChomozygous113351483
141412127514121276AG34GENIChomozygous113351487
141412261114122612GT20GENIChomozygous113659177
141412321414123215GA21GENIChomozygous113907778
141412444414124445AG24GENIChomozygous113659181
141412501514125016CT14GENIChomozygous113659183
141412526814125269CT18GENIChomozygous113907780
141412570014125701CT25GENIChomozygous113659185
141412760114127602AT24GENIChomozygous113718844
141412868714128688GA25GENIChomozygous113907782
141412962414129625GA18GENIChomozygous113718846
141411116214111163AT27GENIChomozygous113575786