chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1241143368241143369GA45GENIChomozygous108591036
1241143827241143828AC60GENIChomozygous108591037
1241144255241144256AT54GENIChomozygous108591038
1241144639241144640GT29GENIChomozygous108591039
1241147886241147887GT48GENICpossibly homozygous108591040
1241148088241148089CA28GENIChomozygous108591041
1241153934241153935AT20GENIChomozygous108591042
1241161606241161607GT4GENIChomozygous108591043
1241185837241185838AC32GENIChomozygous108591044
1241185853241185854AC30GENIChomozygous108591045
1241199010241199011AC48GENIChomozygous108591046
1241191602241191603AC68GENICheterozygous108773969
1241191604241191605AG66GENICheterozygous108773970
1241195932241195933CA141GENICheterozygous108773971
1241216199241216200AC43GENIChomozygous108773972
1241216317241216318AT56GENIChomozygous108591047