chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
138500842085008421CT24GENICheterozygous50264168
138501892585018926CT18GENICheterozygous50264172
138502466985024670AG25GENICheterozygous50264180
138502469085024691GGT20GENICheterozygous49843486
138502481385024814TA6GENICheterozygous49843494
138502481685024817TG6GENICheterozygous49843495
138502482285024823AC6GENICheterozygous49843496
138502748485027485GA29GENICheterozygous50118820
138505361085053611TA34GENICheterozygous49843538
138505395085053951CG36GENICheterozygous49843540
138507134785071350TAA---23GENICheterozygous50118979
138507134885071350AA--23GENICheterozygous51287011
138507152585071526A-21GENICheterozygous50264198
138507242285072423A-21GENICheterozygous50118983
138507242885072429GA17GENICheterozygous50264199
138508118885081189AAT57GENICheterozygous50119056
138510286285102863GA13GENICheterozygous50264235
138511299985113000TG24GENICheterozygous50264240
138514262385142624AC43GENICheterozygous50119374
138514973985149740TC29GENICheterozygous50119463
138516061085160611GA13GENICheterozygous50119584
138526110185261102TC194GENICheterozygous49843891
138526173185261732AC71GENICheterozygous50119908
138526219385262194AG47GENICheterozygous49843893
138526923885269239GA41GENICheterozygous50119933
138526960685269607AAT21GENICheterozygous50119935
138527016285270163GA11GENICheterozygous50119937