chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5166410028166410029GA6GENICheterozygous126315574
5166410221166410222TC8GENIChomozygous119205880
5166410601166410602TC13GENIChomozygous114279375
5166410862166410863GA10GENIChomozygous114279381
5166412017166412018CG10GENIChomozygous114279383
5166412214166412215CT5GENIChomozygous114279385
5166412412166412413CT12GENIChomozygous114279387
5166412537166412538AG10GENIChomozygous114279389
5166416212166416213GC12GENICheterozygous114279393
5166416337166416338TC11GENIChomozygous114279395
5166416355166416356AT10GENIChomozygous114279397
5166416361166416362TC13GENIChomozygous114279399
5166416718166416719TG15GENIChomozygous126207365
5166416822166416823CT5GENIChomozygous126207366
5166416844166416845TA4GENIChomozygous114081952
5166416855166416856GC4GENIChomozygous126207367
5166417117166417118TC13GENIChomozygous114279403
5166419626166419627TC8GENIChomozygous114279413
5166419685166419686GC10GENIChomozygous114279415
5166419786166419787CT11GENIChomozygous114279417
5166420543166420544GA16GENIChomozygous119205881
5166420687166420688GA9GENICheterozygous114279419
5166420715166420716CT10GENIChomozygous114279421
5166421333166421334TA11GENIChomozygous114279423
5166421556166421557AT11GENIChomozygous114279425
5166421743166421744AG12GENIChomozygous114279427
5166422044166422045CT9GENIChomozygous114279429
5166422168166422169CT9GENICheterozygous119205882
5166423917166423918CG8GENIChomozygous114279431
5166424714166424715GC9GENIChomozygous114279435
5166426495166426496GA21GENIChomozygous119205883
5166427610166427611CT6GENIChomozygous119205884