chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
995794729579473CT25GENIChomozygous593945250
995820299582030CCA3GENICheterozygous726185996
995854589585459TTC13GENICheterozygous726185998
995881049588105CT19GENIChomozygous593945251
995884589588459AC26GENIChomozygous593945252
995891849589185G-16GENIChomozygous726185999
995942079594208GGT27GENICpossibly homozygous726186000
996008339600834C-20GENIChomozygous726186001
996036099603610TC19GENICpossibly homozygous593945253
996076249607625GGA13GENICheterozygous726186003
996135579613558TTC10GENIChomozygous726186004
996149809614982TT--14GENICpossibly homozygous726186006
996150059615006CT17GENIChomozygous593945254
996153869615387AT25GENIChomozygous593945255
996195799619580CCCA24GENIChomozygous726186008
996195829619583G-26GENIChomozygous726186009
996195849619585TTCA26GENIChomozygous726186010
996195859619586GC26GENIChomozygous593945256
996205209620521AG25GENIChomozygous593945257
996251939625194TG27GENIChomozygous593945258
996252029625203CCT22GENIChomozygous726186011
996252389625243TTTTT-----8GENIChomozygous726186012
996269829626989GCCCCGG-------3GENIChomozygous726186015
996270239627024AAGTCTCG13GENIChomozygous726186016
996307999630800TTCA8GENICheterozygous726186018
996307999630800TTCACACACA8GENICpossibly homozygous726186019
996327209632721AG23GENIChomozygous593945259
996340709634071C-6GENICheterozygous726186021
996340729634085CACACACACACAC-------------6GENICheterozygous726186022
996356559635657GT--14GENICheterozygous726186024
996372449637245CA26GENIChomozygous593945260