chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4203337274203337275A-6GENIChomozygous57053616
4203338024203338025GA10GENICpossibly homozygous57053617
4203338388203338389TTTTA7GENICheterozygous57053618
4203341223203341224GT23GENICpossibly homozygous57053619
4203341467203341468GT7GENICpossibly homozygous57053620
4203341788203341789AC35GENIChomozygous57053621
4203343085203343086TC12GENIChomozygous57053622
4203343366203343367TC23GENICpossibly homozygous57053623
4203344213203344218GAAAA-----10GENIChomozygous57053624
4203344542203344543TC18GENIChomozygous57053625
4203345474203345475TA14GENIChomozygous57053629
4203345596203345597AT16GENICpossibly homozygous57053630
4203346063203346064TTA2GENIChomozygous57053631
4203346710203346711TC23GENICpossibly homozygous57053632
4203347690203347691T-5GENICheterozygous57053634
4203349891203349892GA24GENICpossibly homozygous57053635
4203350366203350367CA14GENIChomozygous57360508
4203353040203353041CA18GENICpossibly homozygous57053636
4203353929203353931TG--2GENICheterozygous57053637
4203354957203354958TC16GENICpossibly homozygous57053638
4203353931203353932TC2GENICheterozygous58301630