chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3107979833107979834AC48GENIChomozygous146718443
3107982332107982333GA52GENIChomozygous146718444
3107982676107982677CT55GENIChomozygous146718445
3107982990107982991GC39GENIChomozygous136784596
3107982348107982349AG54GENIChomozygous136784595
3107982308107982309TC50GENIChomozygous136784594
3107983165107983166CT35GENIChomozygous136784597
3107983202107983203CT46GENIChomozygous146718446
3107983662107983663CT48GENIChomozygous136784598
3107983733107983734CT49GENIChomozygous136784599
3107984090107984090C60GENIChomozygous136582631
3107984375107984376GA35GENIChomozygous136784600
3107985763107985764G33GENICheterozygous145204564
3107986294107986295CT51GENIChomozygous146718447
3107986637107986638GC59GENIChomozygous146718448
3107984782107984783G48GENIChomozygous146696389
3107987220107987221TC43GENIChomozygous136784601
3107987406107987407GA47GENIChomozygous146718450
3107989174107989175A58GENIChomozygous136582633
3107989721107989722AG60GENIChomozygous136784606
3107985763107985764GA33GENICpossibly homozygous403073262
3107987592107987593GA55GENIChomozygous136784602
3107988213107988214CA61GENIChomozygous136784603
3107988502107988503AG49GENIChomozygous136784604
3107989099107989100AG56GENIChomozygous136784605
3107990115107990116GT41GENIChomozygous146718451
3107990218107990219TC54GENIChomozygous136784607
3107991367107991368A49GENIChomozygous136582634
3107992196107992197AT34GENIChomozygous136784608
3107992698107992699CT55GENIChomozygous136784609
3107993684107993685CT37GENIChomozygous136784610
3107993915107993916CT46GENIChomozygous146718452
3107994174107994175GC47GENICpossibly homozygous136784611
3107995931107995932GA48GENIChomozygous146718453
3107996009107996010GT47GENIChomozygous136784612
3107996126107996127TC58GENIChomozygous136784614
3107996184107996185GA54GENICpossibly homozygous136784615
3107997077107997078CT38GENIChomozygous136784619
3107997876107997877AG51GENIChomozygous136784621