chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8128800050128800051GT14GENIChomozygous52886977
8128801364128801365AG16GENIChomozygous52886978
8128801696128801697AAT18GENIChomozygous52886979
8128803490128803507GCCTGGGTCTGTGCATC-----------------14GENIChomozygous52886982
8128803702128803703GGA12GENIChomozygous52886983
8128803705128803706TA12GENIChomozygous53369604
8128803706128803707GGCAC12GENIChomozygous52886984
8128803754128803755CT15GENIChomozygous52886985
8128804165128804166AG16GENIChomozygous52886986
8128804687128804688AG15GENIChomozygous52886987
8128804949128804950AG12GENIChomozygous52886988
8128805055128805056TC14GENIChomozygous52886989
8128806345128806346AT8GENIChomozygous52886990
8128806917128806918GA15GENIChomozygous52886991
8128807350128807351CT7GENIChomozygous52886992
8128808346128808347TC12GENIChomozygous52886996
8128809380128809381GA14GENIChomozygous52886997
8128810072128810073TG12GENIChomozygous52886998
8128810546128810547GA12GENICpossibly homozygous52886999
8128811208128811209TG8GENIChomozygous52887000
8128811212128811213TG8GENIChomozygous52887001
8128811214128811215TG8GENIChomozygous52887002
8128811224128811225TG11GENIChomozygous52887003
8128811226128811227TG11GENIChomozygous52887004
8128813274128813275TC12GENIChomozygous52887006
8128813286128813287CT13GENIChomozygous52887007
8128813866128813867CCT11GENIChomozygous52887008
8128814029128814030GA14GENIChomozygous52887009
8128814505128814507AA--11GENIChomozygous52887010
8128814892128814893TTA11GENICheterozygous52887011
8128816936128816938AG--11GENIChomozygous52887012
8128820223128820224CT22GENIChomozygous52887016
8128820520128820521AC16GENIChomozygous52887017
8128822299128822300CT11GENIChomozygous52887018
8128824499128824500CG7GENIChomozygous52887019
8128811205128811206TA10GENICheterozygous54349671