chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1153732871153732872CT19GENIChomozygous108314037
1153733082153733083TA13GENIChomozygous108314039
1153734772153734773TC24GENIChomozygous108314041
1153734838153734839AG25GENIChomozygous108314043
1153735543153735544TC20GENIChomozygous108314045
1153736357153736358AG24GENIChomozygous108314047
1153736402153736403TC21GENIChomozygous108314049
1153736674153736675CT16GENIChomozygous108314051
1153736727153736728CT16GENIChomozygous108314053
1153736810153736811AG26GENIChomozygous108314055
1153737190153737191CT18GENIChomozygous108314057
1153737441153737442AG18GENIChomozygous108314059
1153737513153737514AG18GENIChomozygous108314061
1153737900153737901TC15GENIChomozygous108314065
1153737993153737994CG21GENIChomozygous108314067
1153738959153738960TA14GENIChomozygous108314069
1153739438153739439GA18GENIChomozygous108314071
1153740013153740014TA20GENIChomozygous108314073
1153740048153740049CG23GENIChomozygous108314075
1153740478153740479CT29GENIChomozygous108314077
1153740675153740676AG15GENIChomozygous108314079
1153741458153741459TC19GENIChomozygous108314081
1153741645153741646CA12GENIChomozygous108314083
1153741772153741773CA15GENIChomozygous108314095
1153735587153735589GC19GENIChomozygous127447453
1153740978153740978C6GENIChomozygous127447454