chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
139922396499223966AC18GENICheterozygous141041808
139923885499238856TG12GENICheterozygous141041809
139930678499306784ACAG10GENICheterozygous139189518
139936171499361716TG16GENICheterozygous147012982
139938321099383211CG12GENICpossibly homozygous403347273
139938321099383211C12GENICheterozygous403347274
139947127599471277AC22GENICheterozygous144441764
139949744199497442G7GENIChomozygous403347284
139949744199497442GA7GENICheterozygous403347285
139956386999563870G16GENICheterozygous403347288
139956386999563870GC16GENICpossibly homozygous403347289
139959469699594698GT15GENICheterozygous139189520
139936812299368123T22GENICheterozygous141096264
139938321699383217CG12GENICpossibly homozygous140912450
139944016199440162AG6GENICheterozygous139362622
139944373799443738AG9GENIChomozygous139362623
139946911599469116AG11GENIChomozygous139362624
139952667899526680AC17GENICheterozygous141096265
139964007099640071G9GENICheterozygous404024882
139964007099640071GA9GENICheterozygous404024883
139964387499643875AT10GENIChomozygous139362628
139967706599677066TC11GENICpossibly homozygous403650546
139967706599677066T11GENICheterozygous403650547
139967707699677077GA15GENICheterozygous403650548