chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
138532235385322354TG43GENIChomozygous505366433
138532236285322363AC39GENIChomozygous501566352
138532243785322458GTCCACCAGGTAAATCTCAAC---------------------20GENIChomozygous684588445
138532271485322715TTGAGA22GENIChomozygous684588446
138532273985322740GGAGAA28GENICheterozygous684588448
138532275985322761TA--37GENIChomozygous684588449
138532295085322952AC--13GENICpossibly homozygous684588450
138532316385323164AG51GENIChomozygous501566353
138532359985323600AG32GENIChomozygous501566354
138532367485323675TTC36GENIChomozygous684588451
138532418785324188TA4GENIChomozygous505366434
138532420285324203CT1GENIChomozygous501566355
138532421185324212A-1GENIChomozygous684588452
138532421185324212AAT1GENIChomozygous684588453
138532423185324232CT2GENIChomozygous505366435
138532424485324246AC--2GENIChomozygous684588454
138532426585324266GC3GENIChomozygous505366436
138532452985324530GA51GENICpossibly homozygous505366437
138532458185324582GA61GENIChomozygous505366438
138532470985324710AG48GENIChomozygous501566356
138532474685324747TA44GENIChomozygous505366439
138532491285324913GA49GENIChomozygous501566357
138532549185325492TC51GENIChomozygous501566358
138532549285325493AC50GENIChomozygous501566359
138532806285328063CT44GENIChomozygous505366440
138532915985329160CT40GENIChomozygous505366441
138532916185329162AG43GENIChomozygous505366442
138532931785329323CGCGCG------17GENIChomozygous684588455
138532978685329787CT47GENIChomozygous505366443
138532982285329823GA49GENIChomozygous505366444
138533001985330020CT49GENIChomozygous505366445
138533009985330100CT44GENIChomozygous505366446
138533014585330146AAAGTACCTAG31GENIChomozygous684588456
138533027185330272AC44GENIChomozygous505366447
138533046885330469T-42GENIChomozygous684588457
138533163485331635AAT20GENIChomozygous684588458
138533177785331778TC46GENIChomozygous505366448
138533309485333095GA39GENIChomozygous505366449