chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4182308805182308806CT13GENIChomozygous57023398
4182309389182309390GC22GENIChomozygous59157428
4182310072182310073TC29GENIChomozygous57558267
4182310392182310393CT29GENIChomozygous57023400
4182311015182311016GA19GENIChomozygous57558271
4182311719182311720TG22GENIChomozygous57023401
4182312658182312659TTTG13GENIChomozygous57558275
4182312719182312720GGGTGT7GENICheterozygous57023403
4182312720182312722GT--7GENICpossibly homozygous58484018
4182313084182313104TCCATCCATCCATCCGTCCG--------------------6GENIChomozygous59009337
4182313158182313159CT28GENIChomozygous59157430
4182313522182313523GA27GENIChomozygous59157432
4182313878182313879AG12GENIChomozygous57558281
4182313879182313880TTTTCTTCTTCTTC12GENIChomozygous58359599
4182314033182314034GA11GENIChomozygous59157434
4182314427182314428AG20GENIChomozygous57023404
4182314532182314533GA27GENIChomozygous57023405
4182314807182314808AG26GENIChomozygous59157436
4182314931182314932GA23GENIChomozygous59157438
4182315156182315157GA31GENIChomozygous59157440
4182315316182315317AG30GENIChomozygous59157442
4182315710182315711TC15GENIChomozygous57023407
4182316131182316132AG19GENIChomozygous57023408
4182316408182316409TC20GENIChomozygous57558283
4182316846182316847TC19GENIChomozygous57558285
4182317286182317287AG15GENIChomozygous57558287
4182317497182317498CT8GENIChomozygous57558291
4182317618182317619GGA15GENIChomozygous57558293
4182317751182317752GA14GENIChomozygous57558295
4182318011182318012AG16GENIChomozygous57558299
4182318415182318416GC25GENIChomozygous57558301
4182318616182318617TA16GENIChomozygous57558307