chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4117042005117042006TC30GENIChomozygous143149399
4117042408117042409GA15GENIChomozygous145490289
4117042693117042694GT35GENIChomozygous145490290
4117042729117042730GT33GENIChomozygous145490291
4117042894117042894GA22GENIChomozygous145444703
4117042930117042931CA23GENIChomozygous145490292
4117043045117043046TG18GENIChomozygous145490293
4117043452117043453GA23GENIChomozygous145490294
4117043576117043577GA30GENIChomozygous145490295
4117044301117044301C7GENIChomozygous145444704
4117044479117044480AC17GENIChomozygous145490296
4117045143117045144CT26GENIChomozygous145490297
4117045261117045262TC25GENIChomozygous145490298
4117045262117045263TG25GENIChomozygous145490299
4117046474117046475AG21GENIChomozygous145490300
4117047255117047263CTCTCATC38GENIChomozygous145444705
4117047642117047643AG24GENIChomozygous145490301
4117047855117047856AT23GENIChomozygous145490302
4117047856117047857AC23GENIChomozygous145490303
4117048854117048855AT31GENIChomozygous145490304
4117048952117048953CT28GENIChomozygous145490305
4117049697117049698AG19GENIChomozygous145490306
4117050280117050281CT18GENIChomozygous145490307
4117050509117050510CT27GENIChomozygous145490308
4117050737117050738CT32GENIChomozygous145490309
4117050856117050857AG35GENIChomozygous145490310
4117051131117051132AG26GENIChomozygous145490311
4117051270117051271TC31GENICpossibly homozygous145490312
4117051471117051472GA20GENIChomozygous145490313
4117052370117052371AC19GENICpossibly homozygous145490314
4117053550117053605TTCCTTTTCTTTCCTTTTCTTTCCTTTTCTTTCCTTTCCTTTTCTTTTCTTTTCC25GENIChomozygous145444706
4117055531117055532CG21GENIChomozygous145490315
4117055859117055861CT18GENIChomozygous145444707
4117057232117057233AT21GENIChomozygous145490316
4117057395117057396AG20GENIChomozygous145490317
4117057859117057860CT15GENIChomozygous145490318