chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7111622458111622461CCC28GENIChomozygous137974397
7111622463111622466GGG28GENIChomozygous137974398
7111622635111622636AG52GENIChomozygous138182639
7111623323111623324AG55GENIChomozygous138182640
7111623331111623332GC57GENIChomozygous138182641
7111623352111623353CT52GENIChomozygous138182642
7111623392111623393TC38GENIChomozygous138182643
7111623564111623565AG50GENIChomozygous138182644
7111624064111624065CT54GENIChomozygous138182645
7111624473111624474AG35GENIChomozygous138182646
7111624507111624508AG42GENIChomozygous138182647
7111624682111624683TC35GENIChomozygous138182648
7111624880111624881TC51GENICpossibly homozygous138182649
7111625144111625145TG55GENIChomozygous138182650
7111625407111625408CG39GENICpossibly homozygous138182651
7111626450111626451GA48GENIChomozygous138182652
7111626876111626877CG46GENIChomozygous138182653
7111626907111626908CG43GENIChomozygous138182654
7111626930111626931CA47GENIChomozygous138182655