chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
187757260277572603CT14GENIChomozygous110411221
187757284577572846GA13GENIChomozygous110411223
187757315677573157GA24GENIChomozygous110411225
187757360577573606CA12GENICpossibly homozygous110411227
187757476577574766GC21GENIChomozygous110411231
187757546577575466CT17GENIChomozygous110411235
187757556977575570TC19GENIChomozygous110411237
187757676277576763TC19GENIChomozygous110411239
187758285077582851CG18GENIChomozygous110411241
187758547977585480GA18GENIChomozygous110733564
187758146977581470GT25GENIChomozygous110733560
187758211977582120AG21GENIChomozygous110733562
187758474277584743CA18GENIChomozygous110636946
187758480877584809GA28GENIChomozygous110636948
187758396077583972CTTTCTTTCTTC14GENIChomozygous131209836
187758569877585699TC21GENIChomozygous110733566
187758571777585718CG23GENIChomozygous110733568
187758604577586055TCCTTTCTAC12GENIChomozygous131209837
187758675277586753GA26GENIChomozygous110636950
187758719077587191GC20GENIChomozygous110636952
187758731477587315CT20GENIChomozygous110636954
187758754377587544GA19GENIChomozygous110636956
187758785877587859TC17GENIChomozygous110636958
187758809677588097CA20GENIChomozygous110636960
187758813977588140TG20GENIChomozygous110733570
187758843777588438GA15GENIChomozygous110636962
187758858277588583AG18GENIChomozygous110636964
187758942277589423GA15GENIChomozygous110636966
187758942777589428TG16GENIChomozygous110636968
187758973077589731AG18GENIChomozygous110636970
187759142577591426AG6GENIChomozygous110636972
187758561977585620A15GENIChomozygous129555547
187758603177586032GA15GENIChomozygous110758200
187758603377586034CA15GENIChomozygous110758202