chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5159590044159590045CT19GENIChomozygous114072974
5159590377159590378GA12GENIChomozygous114072977
5159590516159590517AG4GENIChomozygous114072978
5159590543159590544TC8GENIChomozygous114072979
5159590567159590568TC6GENIChomozygous114072980
5159590810159590811GA5GENIChomozygous114072981
5159591041159591042CT25GENIChomozygous114072983
5159591165159591166AG18GENIChomozygous114072984
5159591294159591295GA14GENIChomozygous114072985
5159591492159591493CT10GENICheterozygous114072986
5159591711159591712GA14GENIChomozygous114072987
5159591959159591960CT12GENIChomozygous114072988
5159592241159592242AG21GENIChomozygous114072989
5159592551159592552GA12GENIChomozygous114072990
5159592593159592594GA21GENIChomozygous114072991
5159592713159592714CT11GENIChomozygous114072992
5159593011159593012TA8GENIChomozygous114072993
5159593229159593230AG15GENIChomozygous114072994
5159593316159593317AC11GENIChomozygous114072995
5159594481159594482GA16GENIChomozygous114072996
5159595521159595522GA11GENIChomozygous114072997
5159598268159598269GA12GENIChomozygous114072998
5159599504159599505TC24GENIChomozygous114072999
5159600471159600472TC21GENIChomozygous114073000
5159601143159601144CT22GENIChomozygous114073001
5159601217159601218AG12GENIChomozygous114073002
5159601274159601275AG12GENIChomozygous114073003
5159602018159602019CT6GENIChomozygous114073004