chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103878264838782649CG40GENIChomozygous116762496
103878279838782799GA35GENIChomozygous117004388
103878309538783096AG34GENIChomozygous116925226
103878321338783214GA47GENIChomozygous116762498
103878340738783408TA44GENIChomozygous116762500
103878341838783419AC42GENIChomozygous116762502
103878341938783420GA41GENIChomozygous116762504
103878343038783431AG40GENIChomozygous116762506
103878444838784449TC43GENIChomozygous117004390
103878452238784523AG46GENIChomozygous117312372
103878494938784950CA41GENICpossibly homozygous117409782
103878495638784957AG42GENIChomozygous117194058
103878516838785169TC19GENIChomozygous118065737
103878516938785170GT19GENICheterozygous134343305
103878571638785717CA2GENIChomozygous132332866
103878580938785810GA7GENICheterozygous132332867
103878585038785851CT8GENICheterozygous132332868
103878614138786142TA9GENICheterozygous134142720
103878619538786196CT10GENICheterozygous131100897
103878641538786416GT12GENICheterozygous132332870
103878711238787113GA16GENICheterozygous131100899
103878768238787683CT13GENIChomozygous131100900
103878791638787917CT39GENIChomozygous117194059
103878849938788500AG46GENIChomozygous116762510
103878857738788577AAAC42GENIChomozygous131091468
103878586438785864G7GENICheterozygous132331130
103878607938786080T13GENICheterozygous130681707
103878730438787305T6GENIChomozygous131091463
103878730638787308AT6GENIChomozygous131091464
103878769038787691T15GENIChomozygous131091465
103878769338787695AT15GENIChomozygous131091466
103878793738787937TAAAA34GENIChomozygous131091467
103878965638789657T50GENIChomozygous131091469
103879025738790258GT40GENIChomozygous116762512
103879063538790636CG42GENIChomozygous117344097
103879113638791137TG41GENICpossibly homozygous131472383
103879120538791206TC47GENIChomozygous117150864
103879151638791517AT48GENIChomozygous116762514
103879156638791567CT42GENIChomozygous116762516
103879183538791835TATGG44GENIChomozygous131091470
103879184038791841GA48GENIChomozygous116762518