chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1165666627165666628TC26GENIChomozygous108354982
1165667106165667107AG25GENIChomozygous108354984
1165667142165667143CT25GENIChomozygous108354986
1165668162165668163TC37GENIChomozygous108354988
1165668377165668378GC37GENIChomozygous108354990
1165669218165669219TC36GENIChomozygous108354992
1165669673165669674TC35GENIChomozygous108354994
1165669816165669817AG16GENIChomozygous108354996
1165670189165670190CT23GENIChomozygous108354998
1165670556165670557CT30GENIChomozygous108355000
1165671013165671014GA31GENIChomozygous108355002
1165671577165671578CT22GENIChomozygous108355004
1165671992165671993CT12GENIChomozygous108355006
1165672275165672276TC21GENIChomozygous108355008
1165672594165672595CT19GENIChomozygous108355010
1165672742165672743GA23GENIChomozygous108355012
1165673217165673218GA21GENIChomozygous108355014
1165673785165673786CT24GENIChomozygous108355016
1165674096165674097TC35GENIChomozygous108355018
1165674199165674200CT30GENIChomozygous108355020
1165674241165674242TC39GENIChomozygous108355022
1165674523165674524AC37GENIChomozygous108355024
1165675934165675935GA23GENIChomozygous108355026
1165675971165675972TC22GENIChomozygous108355028
1165676699165676700CT16GENIChomozygous108355032
1165676962165676963AG3GENIChomozygous108355034
1165678217165678218GA16GENIChomozygous108355036
1165680132165680133CT17GENIChomozygous108355038
1165680330165680331AG14GENIChomozygous108355040
1165681593165681594TA7GENICheterozygous120906569
1165681795165681796CT17GENIChomozygous108355042
1165683004165683005GA29GENIChomozygous108355044
1165683022165683023AC30GENIChomozygous108355046
1165683041165683042AG32GENIChomozygous108355048
1165683274165683275TA21GENIChomozygous108355050