chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X128434025128434025T15GENICpossibly homozygous129789343
X128434327128434327T14GENIChomozygous129789344
X128435366128435370CAGA5GENIChomozygous129789345
X128435572128435573GA18GENIChomozygous108332004
X128435821128435822GA15GENIChomozygous108332006
X128437301128437302AG21GENIChomozygous108332008
X128437884128437885TC16GENIChomozygous108332010
X128440980128440981TC27GENIChomozygous108332012
X128443267128443268AG20GENIChomozygous108332014
X128443720128443721CA21GENIChomozygous108332016
X128444187128444188CG5GENIChomozygous129828058
X128444189128444190CG5GENIChomozygous129828059
X128444191128444192CG5GENIChomozygous129828060
X128444193128444194CG5GENIChomozygous129828061
X128445673128445674CT17GENIChomozygous108332019
X128447089128447090GA23GENIChomozygous108332021
X128447967128447968GA31GENIChomozygous108332023
X128449075128449075CACG11GENIChomozygous129789347
X128449215128449216CT15GENIChomozygous108332025
X128450408128450409CT26GENIChomozygous108332027
X128451628128451629GA15GENIChomozygous108332029
X128452566128452567AG23GENIChomozygous108332031
X128452712128452713AG22GENIChomozygous108332033
X128454697128454697A22GENIChomozygous129789349
X128454811128454811T27GENIChomozygous129789350
X128455314128455315AG20GENIChomozygous108332035
X128455486128455487GA19GENIChomozygous108332037
X128455588128455589TC26GENIChomozygous108332039
X128455645128455646GT27GENIChomozygous108332041