chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
176969592869695929AT36GENICpossibly homozygous782792994
176969781969697820GA75GENICpossibly homozygous782792995
176969798469697985CT73GENIChomozygous782792996
176969870469698705TC73GENICpossibly homozygous782792997
176969885769698858AG74GENIChomozygous782792998
176969939669699397GA39GENICpossibly homozygous782792999
176969940469699405TG37GENICpossibly homozygous782793000
176969950369699504AG34GENIChomozygous782793001
176970099469700995CT54GENICpossibly homozygous782793002
176970127169701272CT63GENIChomozygous782793003
176970155369701554GA51GENIChomozygous782793004
176970199069701991GA88GENICheterozygous782793005
176970200069702001CG97GENICheterozygous782793006
176970206669702067TC105GENICheterozygous782793007
176970208469702085AG97GENICheterozygous782793008
176970243469702435CA83GENICheterozygous782793009
176970294369702944TC72GENIChomozygous782793010
176970305469703055CA103GENICheterozygous782793011
176970306169703062AT104GENICheterozygous782793012
176970306869703069AT112GENICheterozygous782793013
176970307169703072CA110GENICheterozygous782793014
176970307569703076TC115GENICheterozygous782793015
176970308269703083CA126GENICheterozygous782793016
176970311669703117AC138GENICheterozygous782793017
176970312969703130GA124GENICheterozygous782793018
176970316269703163GT100GENICheterozygous782793019
176970333869703339GT83GENICpossibly homozygous782793020
176970353769703538GT187GENICheterozygous782793021
176970361069703611AT232GENICheterozygous782793022
176970362969703630GC250GENICheterozygous782793023
176970374969703750AG244GENICheterozygous782793024
176970450469704505GA51GENICpossibly homozygous782793025
176970917969709180TC71GENICpossibly homozygous782793026
176971133369711334TG44GENIChomozygous782793027