chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1265810464265810465G16GENIChomozygous127508931
1265812073265812074TC21GENIChomozygous108637307
1265812439265812440TC18GENIChomozygous108637308
1265813330265813331TG21GENIChomozygous108637309
1265813411265813412GA22GENIChomozygous108637310
1265813509265813510GT14GENIChomozygous108637311
1265813563265813564AT16GENIChomozygous108637312
1265813569265813570AG16GENIChomozygous108637313
1265813678265813679AT9GENIChomozygous108637314
1265813935265813936TC16GENIChomozygous108637315
1265814481265814481C13GENIChomozygous127508932
1265814680265814681TC23GENIChomozygous108637316
1265817456265817457AG23GENIChomozygous108637317
1265818586265818587CT13GENIChomozygous108637318
1265819020265819021GA19GENIChomozygous108637319
1265819282265819283TC25GENIChomozygous108637320
1265819772265819773CG23GENIChomozygous108637321
1265819832265819833TG23GENIChomozygous108637322
1265819865265819866TA19GENICpossibly homozygous108637323
1265820899265820900AG11GENIChomozygous108637324
1265820997265820998AT13GENIChomozygous108637325
1265821200265821201GA11GENIChomozygous108637326
1265823543265823544AG25GENIChomozygous108637327
1265823822265823823C13GENIChomozygous127508933
1265825187265825187A14GENIChomozygous127508934
1265825216265825217G15GENIChomozygous127508935