chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104835903948359040GA23GENIChomozygous52055441
104836009148360092AG28GENIChomozygous51639309
104836137748361378AAGAGATTGATTGATT1GENIChomozygous52459734
104836216648362167CT36GENIChomozygous51639313
104836258748362588A-13GENICpossibly homozygous52055443
104836266048362661TC25GENIChomozygous51639314
104836374248363743CG21GENIChomozygous52055446
104836448348364484GA25GENIChomozygous52055448
104836548048365481TC29GENIChomozygous51639323
104836553948365540AG29GENIChomozygous51639324
104836718948367190CCA1GENIChomozygous52318293
104836890348368904CG23GENIChomozygous51639329
104836904448369045AAT18GENIChomozygous51446988
104836933048369331GT23GENIChomozygous51639330
104837004648370047CT27GENIChomozygous52055450
104837006548370066TC25GENIChomozygous52055452
104837127648371277CT41GENIChomozygous51639334
104837310348373104GGGTTTT33GENIChomozygous51639335
104837312548373126TTTTG25GENICpossibly homozygous51639336
104837331348373314TC29GENIChomozygous51639337
104837399848373999GA28GENIChomozygous51639338