chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8128800050128800051GT18GENICheterozygous52886977
8128801364128801365AG7GENIChomozygous52886978
8128801696128801697AAT19GENIChomozygous52886979
8128803490128803507GCCTGGGTCTGTGCATC-----------------4GENICheterozygous52886982
8128803702128803703GGA7GENIChomozygous52886983
8128803705128803706TA7GENIChomozygous53369604
8128803706128803707GGCAC5GENIChomozygous52886984
8128803754128803755CT22GENICheterozygous52886985
8128804165128804166AG24GENICpossibly homozygous52886986
8128804687128804688AG17GENIChomozygous52886987
8128804949128804950AG19GENICpossibly homozygous52886988
8128805055128805056TC18GENICpossibly homozygous52886989
8128806345128806346AT11GENICpossibly homozygous52886990
8128806917128806918GA32GENICpossibly homozygous52886991
8128807350128807351CT26GENICheterozygous52886992
8128808346128808347TC23GENIChomozygous52886996
8128809380128809381GA15GENICpossibly homozygous52886997
8128810072128810073TG29GENIChomozygous52886998
8128810546128810547GA10GENIChomozygous52886999
8128811224128811225TG3GENIChomozygous52887003
8128811226128811227TG3GENIChomozygous52887004
8128811519128811520GGTT1GENIChomozygous52887005
8128812750128812751A-1GENIChomozygous53064661
8128813274128813275TC12GENIChomozygous52887006
8128813286128813287CT11GENICpossibly homozygous52887007
8128813866128813867CCT19GENICpossibly homozygous52887008
8128814029128814030GA25GENICpossibly homozygous52887009
8128814505128814507AA--2GENIChomozygous52887010
8128816936128816938AG--18GENIChomozygous52887012
8128817512128817513GT3GENIChomozygous52887015
8128820223128820224CT26GENIChomozygous52887016
8128820520128820521AC9GENIChomozygous52887017
8128822299128822300CT23GENICpossibly homozygous52887018
8128824499128824500CG26GENICpossibly homozygous52887019
8128825337128825338T-2GENICheterozygous53455911