chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
151183668611836687A20GENIChomozygous129229768
151183688511836886CT15GENIChomozygous112451102
151184446111844462CA11GENIChomozygous118869451
151184447611844477T11GENIChomozygous129229770
151184448211844482G10GENIChomozygous129229771
151184449111844492A9GENIChomozygous129229772
151184455911844561CA13GENIChomozygous129229773
151184456311844564AC13GENIChomozygous112451115
151184446711844468GT12GENIChomozygous113161651
151184446811844469CG12GENIChomozygous112898924
151185141011851411A19GENIChomozygous129229774
151186498311864983A25GENIChomozygous129229779
151186509311865093T23GENIChomozygous129229780
151187795811877959C3GENIChomozygous129229783
151187797911877980C3GENIChomozygous129229784
151187800611878008TG6GENIChomozygous129229785
151187805811878059TC9GENIChomozygous112898951
151187812911878130C14GENIChomozygous129229786
151189528111895281A13GENIChomozygous129229792
151189529711895298G13GENIChomozygous129229793
151189533811895339A11GENIChomozygous129229794
151189535911895360G8GENIChomozygous129229795
151189538211895383G8GENIChomozygous129229796
151189539811895399T9GENIChomozygous129229797
151189541311895414C10GENIChomozygous129229798
151189543011895432GC13GENIChomozygous129229799
151186508311865084CA24GENIChomozygous112658211
151186966911869670AG12GENIChomozygous112658214