chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8128800050128800051GT7GENICheterozygous52886977
8128801364128801365AG8GENIChomozygous52886978
8128801696128801697AAT20GENICpossibly homozygous52886979
8128803490128803507GCCTGGGTCTGTGCATC-----------------4GENICheterozygous52886982
8128803702128803703GGA4GENIChomozygous52886983
8128803705128803706TA4GENIChomozygous53369604
8128803706128803707GGCAC4GENIChomozygous52886984
8128803754128803755CT27GENIChomozygous52886985
8128804165128804166AG30GENICpossibly homozygous52886986
8128804687128804688AG17GENICpossibly homozygous52886987
8128804949128804950AG21GENICpossibly homozygous52886988
8128805055128805056TC12GENIChomozygous52886989
8128806345128806346AT13GENIChomozygous52886990
8128806917128806918GA22GENIChomozygous52886991
8128807350128807351CT23GENIChomozygous52886992
8128808346128808347TC29GENIChomozygous52886996
8128809380128809381GA14GENIChomozygous52886997
8128810072128810073TG17GENIChomozygous52886998
8128810546128810547GA10GENIChomozygous52886999
8128811224128811225TG1GENIChomozygous52887003
8128811226128811227TG2GENIChomozygous52887004
8128812750128812751A-2GENIChomozygous53064661
8128813274128813275TC13GENIChomozygous52887006
8128813286128813287CT12GENIChomozygous52887007
8128813866128813867CCT19GENIChomozygous52887008
8128814029128814030GA11GENIChomozygous52887009
8128814505128814507AA--3GENICheterozygous52887010
8128814506128814507A-3GENICheterozygous53653078
8128816936128816938AG--18GENIChomozygous52887012
8128817512128817513GT2GENICheterozygous52887015
8128820223128820224CT15GENIChomozygous52887016
8128820520128820521AC10GENIChomozygous52887017
8128822299128822300CT17GENICpossibly homozygous52887018
8128824499128824500CG20GENICpossibly homozygous52887019