chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4203337274203337275A-6GENIChomozygous57053616
4203338024203338025GA7GENIChomozygous57053617
4203338388203338389TTTTA12GENIChomozygous57053618
4203339573203339574TA11GENICheterozygous57873128
4203341223203341224GT18GENIChomozygous57053619
4203341467203341468GT15GENIChomozygous57053620
4203341788203341789AC9GENIChomozygous57053621
4203343085203343086TC12GENIChomozygous57053622
4203343366203343367TC14GENICpossibly homozygous57053623
4203344213203344218GAAAA-----13GENIChomozygous57053624
4203344542203344543TC21GENIChomozygous57053625
4203344814203344816CA--11GENIChomozygous57053626
4203344818203344821CAC---11GENIChomozygous57053627
4203345474203345475TA12GENIChomozygous57053629
4203345596203345597AT22GENIChomozygous57053630
4203346063203346064TTA9GENIChomozygous57053631
4203346710203346711TC13GENIChomozygous57053632
4203347110203347111CCATAT8GENICheterozygous57053633
4203347690203347691T-26GENIChomozygous57053634
4203349891203349892GA23GENIChomozygous57053635
4203350366203350367CA31GENIChomozygous57360508
4203344833203344834AACGCTCG9GENIChomozygous57360502
4203347110203347111CCATATAT8GENICheterozygous57360506
4203353040203353041CA11GENIChomozygous57053636
4203353929203353931TG--11GENIChomozygous57053637
4203354957203354958TC16GENIChomozygous57053638