chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1153732871153732872CT23GENIChomozygous108314037
1153733082153733083TA40GENIChomozygous108314039
1153734772153734773TC27GENIChomozygous108314041
1153734838153734839AG17GENIChomozygous108314043
1153735543153735544TC33GENIChomozygous108314045
1153736357153736358AG33GENIChomozygous108314047
1153736402153736403TC37GENIChomozygous108314049
1153736674153736675CT28GENIChomozygous108314051
1153736727153736728CT34GENIChomozygous108314053
1153736810153736811AG21GENIChomozygous108314055
1153737190153737191CT36GENIChomozygous108314057
1153737441153737442AG31GENIChomozygous108314059
1153737513153737514AG42GENIChomozygous108314061
1153737835153737836GT18GENIChomozygous108314063
1153737900153737901TC21GENIChomozygous108314065
1153737993153737994CG23GENIChomozygous108314067
1153738959153738960TA25GENIChomozygous108314069
1153739438153739439GA30GENIChomozygous108314071
1153740013153740014TA32GENIChomozygous108314073
1153740048153740049CG32GENIChomozygous108314075
1153740478153740479CT25GENIChomozygous108314077
1153740675153740676AG27GENIChomozygous108314079
1153741458153741459TC54GENIChomozygous108314081
1153741645153741646CA29GENIChomozygous108314083
1153741706153741707TC27GENICheterozygous108314085
1153741711153741712TC28GENICheterozygous108314087
1153741716153741717TC27GENICheterozygous108314089
1153741721153741722TC27GENICheterozygous108314091
1153741726153741727TC28GENICheterozygous108314093
1153741772153741773CA32GENICpossibly homozygous108314095