chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106630380266303803AG6GENIChomozygous53152758
106630393966303940GT11GENICpossibly homozygous53152760
106630421866304219GA24GENIChomozygous53188343
106630436166304362GT10GENIChomozygous53188345
106630468166304682GA7GENIChomozygous51479477
106630472566304726AAT2GENIChomozygous51907887
106630491666304920GTCT----6GENIChomozygous51479479
106630499766304998T-18GENIChomozygous51479480
106630528566305286GA28GENIChomozygous51907889
106630610666306107GA25GENIChomozygous51907897
106630646766306468TC18GENICpossibly homozygous51479483
106630661266306613TC13GENIChomozygous51907899
106630747466307475TA6GENICheterozygous51907901
106630770366307704GA20GENICpossibly homozygous51907903
106630837766308378CT2GENICheterozygous51907907
106630845366308454AG4GENIChomozygous51907909
106630848166308482TTA1GENIChomozygous53188346
106630934566309346A-3GENICheterozygous51479488
106630984066309841GA14GENIChomozygous51907913
106630987066309871GA4GENICheterozygous51907915
106631060666310607CA17GENIChomozygous51907919
106631103366311034TA21GENICpossibly homozygous53188350
106631718966317190GA6GENIChomozygous51907921
106631739566317396T-15GENIChomozygous51479490
106631756966317570CT6GENIChomozygous51907923
106631757366317574AG7GENIChomozygous51907925
106631791166317912GA23GENIChomozygous51907927
106631869466318695CT8GENIChomozygous51907929
106631878566318786GA11GENIChomozygous51907931
106631904466319045G-27GENICpossibly homozygous51479494
106631997566319976CCA9GENIChomozygous51479495
106632269766322698AG5GENIChomozygous51479500
106632576166325762CT10GENICpossibly homozygous51479509
106632654466326545CT6GENIChomozygous51479510
106632693666326937TC20GENIChomozygous53188352
106632698466326985GA20GENIChomozygous53188354
106632704766327048AG24GENICpossibly homozygous51479512
106632718966327190AG9GENIChomozygous51479513