chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1153732871153732872CT22GENIChomozygous108314037
1153733082153733083TA23GENIChomozygous108314039
1153734772153734773TC27GENIChomozygous108314041
1153734838153734839AG24GENIChomozygous108314043
1153735543153735544TC32GENIChomozygous108314045
1153736357153736358AG13GENIChomozygous108314047
1153736402153736403TC13GENIChomozygous108314049
1153736674153736675CT27GENIChomozygous108314051
1153736727153736728CT16GENIChomozygous108314053
1153736810153736811AG20GENIChomozygous108314055
1153737190153737191CT10GENIChomozygous108314057
1153737441153737442AG14GENIChomozygous108314059
1153737513153737514AG16GENIChomozygous108314061
1153737835153737836GT21GENIChomozygous108314063
1153737900153737901TC19GENIChomozygous108314065
1153737993153737994CG9GENIChomozygous108314067
1153738959153738960TA18GENIChomozygous108314069
1153739438153739439GA20GENIChomozygous108314071
1153740013153740014TA15GENIChomozygous108314073
1153740048153740049CG9GENIChomozygous108314075
1153740478153740479CT17GENIChomozygous108314077
1153740675153740676AG31GENIChomozygous108314079
1153741458153741459TC27GENIChomozygous108314081
1153741645153741646CA29GENIChomozygous108314083
1153741706153741707TC26GENICheterozygous108314085
1153741711153741712TC26GENICheterozygous108314087
1153741716153741717TC27GENICheterozygous108314089
1153741721153741722TC31GENICheterozygous108314091
1153741726153741727TC31GENICheterozygous108314093
1153741772153741773CA34GENIChomozygous108314095