chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1265810464265810465G15GENIChomozygous127508931
1265812073265812074TC27GENIChomozygous108637307
1265812439265812440TC27GENIChomozygous108637308
1265813330265813331TG24GENIChomozygous108637309
1265813411265813412GA21GENIChomozygous108637310
1265813509265813510GT32GENIChomozygous108637311
1265813563265813564AT36GENIChomozygous108637312
1265813569265813570AG37GENIChomozygous108637313
1265813678265813679AT23GENIChomozygous108637314
1265813935265813936TC27GENIChomozygous108637315
1265814481265814481C15GENIChomozygous127508932
1265814680265814681TC31GENIChomozygous108637316
1265817456265817457AG28GENIChomozygous108637317
1265818586265818587CT14GENIChomozygous108637318
1265819832265819833TG22GENIChomozygous108637322
1265819020265819021GA26GENIChomozygous108637319
1265819282265819283TC29GENIChomozygous108637320
1265819772265819773CG29GENIChomozygous108637321
1265819865265819866TA18GENIChomozygous108637323
1265820899265820900AG27GENIChomozygous108637324
1265820997265820998AT30GENIChomozygous108637325
1265821200265821201GA22GENIChomozygous108637326
1265823543265823544AG25GENIChomozygous108637327
1265823822265823823C23GENIChomozygous127508933
1265825187265825187A14GENIChomozygous127508934
1265825216265825217G19GENIChomozygous127508935