chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
46938484569384846TC19GENIChomozygous112695246
46938902969389030TC42GENIChomozygous112695311
46938910769389108CG35GENICheterozygous112695317
46938917269389173TC32GENIChomozygous112695321
46938938769389388TA34GENICheterozygous112695331
46938956669389567GC20GENICheterozygous112695339
46938988869389889TC65GENICheterozygous112695362
46938919069389191GA29GENICheterozygous113237569
46938952369389524GC23GENICheterozygous119277702
46939031169390312TG49GENIChomozygous112695394
46939034269390343CA49GENICheterozygous112695396
46939037469390375GC48GENICheterozygous113348512
46939039369390394CA53GENICheterozygous113237574
46939043169390432CT53GENICheterozygous113237575
46939044069390441CT54GENICheterozygous113237576
46939060769390608CA35GENICheterozygous119306673
46939081469390815TA45GENICheterozygous112695433
46939082069390821CA48GENICheterozygous112695435
46939083669390837TC49GENICheterozygous112695437
46939083769390838GA52GENICheterozygous112695439
46939097769390978GA51GENICheterozygous112695443
46939108469391085AG68GENIChomozygous113348516
46939110869391109AT64GENICheterozygous112695459
46939142569391426AG55GENICheterozygous112695472
46939152469391525AG52GENIChomozygous112695480
46939154069391541GA52GENICheterozygous113237580