chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
995794729579473CT21GENIChomozygous628585560
995854589585459TTC7GENICheterozygous744645992
995881049588105CT26GENIChomozygous628585561
995884589588459AC32GENIChomozygous628585562
995891849589185G-18GENIChomozygous744645993
995942079594208GGT18GENIChomozygous744645994
996008339600834C-14GENIChomozygous744645995
996036099603610TC35GENIChomozygous628585563
996076249607625GGA6GENICheterozygous744645997
996135579613558TTC15GENIChomozygous744645998
996149809614982TT--14GENIChomozygous744646000
996150059615006CT15GENIChomozygous628585564
996153869615387AT41GENICpossibly homozygous628585565
996195799619580CCCA25GENIChomozygous744646002
996195829619583G-26GENIChomozygous744646003
996195849619585TTCA24GENIChomozygous744646004
996195859619586GC24GENIChomozygous628585566
996205209620521AG27GENIChomozygous628585567
996251939625194TG27GENIChomozygous628585568
996252029625203CCT20GENICpossibly homozygous744646005
996252389625243TTTTT-----1GENIChomozygous744646006
996268099626810AC1GENIChomozygous628585569
996269829626989GCCCCGG-------5GENIChomozygous744646009
996270239627024AAGTCTCG10GENIChomozygous744646010
996307999630800TTCACACACA6GENICheterozygous744646013
996307999630800TTCACACACACA6GENICheterozygous744646014
996327209632721AG23GENIChomozygous628585570
996340709634071C-5GENICheterozygous744646015
996340729634085CACACACACACAC-------------5GENICheterozygous744646016
996372449637245CA24GENIChomozygous628585571