chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4182308727182308728CT34GENIChomozygous57558259
4182308805182308806CT34GENIChomozygous57023398
4182309008182309009CT25GENIChomozygous57558261
4182309829182309830CA16GENIChomozygous57558263
4182309989182309990CT16GENIChomozygous57558265
4182310072182310073TC21GENIChomozygous57558267
4182310392182310393CT32GENIChomozygous57023400
4182310897182310898CT21GENIChomozygous57558269
4182311015182311016GA28GENIChomozygous57558271
4182311719182311720TG22GENIChomozygous57023401
4182311952182311953AG24GENIChomozygous57558273
4182312658182312659TTTG40GENICpossibly homozygous57558275
4182312719182312720GGGT28GENICheterozygous57023402
4182312719182312720GGGTGT28GENICheterozygous57023403
4182312825182312826GA33GENIChomozygous57558277
4182313878182313879AG31GENIChomozygous57558281
4182313879182313880TTTTCTTCTTCTTC30GENIChomozygous58359599
4182314427182314428AG14GENIChomozygous57023404
4182314532182314533GA16GENIChomozygous57023405
4182315710182315711TC28GENIChomozygous57023407
4182316131182316132AG22GENIChomozygous57023408
4182316408182316409TC29GENIChomozygous57558283
4182316846182316847TC39GENIChomozygous57558285
4182317286182317287AG46GENIChomozygous57558287
4182317497182317498CT13GENIChomozygous57558291
4182317618182317619GGA31GENIChomozygous57558293
4182317751182317752GA28GENIChomozygous57558295
4182317868182317869CT36GENIChomozygous57558297
4182318011182318012AG41GENIChomozygous57558299
4182318415182318416GC27GENIChomozygous57558301
4182318530182318531TC21GENIChomozygous57558303
4182318603182318604AG22GENIChomozygous57558305
4182318616182318617TA23GENIChomozygous57558307
4182313084182313104TCCATCCATCCATCCGTCCG--------------------16GENIChomozygous59009337