chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4152430698152430699TC11GENIChomozygous112888179
4152431205152431205TG3GENICheterozygous135107987
4152431208152431209CG2GENIChomozygous134690584
4152431210152431211CG2GENIChomozygous134690585
4152431212152431213CG2GENIChomozygous132973432
4152431214152431215CG2GENIChomozygous132973433
4152431216152431217CG2GENIChomozygous132973434
4152435173152435174TC16GENIChomozygous112888181
4152435992152435993AG20GENIChomozygous112888182
4152438450152438451GA26GENIChomozygous113397495
4152438478152438479AC22GENIChomozygous112888183
4152441183152441184AG20GENIChomozygous112888193
4152441564152441565T20GENIChomozygous134684998
4152442454152442455GA22GENIChomozygous134690587
4152447888152447889AG14GENIChomozygous112888196
4152447909152447910AG13GENIChomozygous112888197
4152447028152447028TG18GENIChomozygous128092368
4152437775152437776CT19GENIChomozygous119576222
4152437846152437847GC23GENIChomozygous119576223
4152441666152441667AC10GENIChomozygous119576224
4152442491152442492GA19GENIChomozygous119576225
4152443995152443996AC28GENIChomozygous119576226
4152444256152444257CT26GENIChomozygous119576227
4152445818152445819AG13GENIChomozygous119576228
4152448631152448632TG17GENIChomozygous112888198
4152450632152450633CG24GENIChomozygous119576229
4152450726152450727AG29GENIChomozygous119576230
4152450955152450956CT24GENIChomozygous119576231