chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3123810776123810777CA27GENICpossibly homozygous111692819
3123810789123810790TC30GENIChomozygous111692820
3123812651123812652AG20GENIChomozygous111692823
3123813010123813011TC35GENIChomozygous111692824
3123813274123813275TG26GENIChomozygous111692825
3123815438123815439TC39GENIChomozygous111692826
3123815616123815617AT26GENIChomozygous111692827
3123816798123816799CA20GENIChomozygous111692828
3123816835123816836CG19GENIChomozygous111692829
3123817195123817196AG12GENIChomozygous111692830
3123817351123817352TC19GENIChomozygous111692831
3123818315123818316AG23GENIChomozygous111692832
3123818393123818394TC28GENIChomozygous111692833
3123818719123818720TC20GENIChomozygous111692834
3123818907123818908GC14GENIChomozygous111692835
3123819654123819655AC27GENIChomozygous111692836
3123821735123821736GA32GENICheterozygous112429542
3123822227123822228CT22GENIChomozygous111692837
3123823045123823046CA21GENIChomozygous111692838
3123823424123823425AG22GENIChomozygous111692839
3123823620123823621AG25GENIChomozygous111692840
3123825492123825493CT40GENIChomozygous111692841
3123826791123826792AT36GENIChomozygous111692842
3123826838123826839CT32GENIChomozygous111692843
3123827159123827160AG17GENIChomozygous111692844
3123827240123827241AC12GENIChomozygous111692845
3123827533123827534TG26GENIChomozygous111692846
3123828564123828565GT18GENIChomozygous111692847
3123829675123829676GT23GENICpossibly homozygous111692848
3123829988123829989GA29GENIChomozygous111692849
3123831014123831015AG34GENIChomozygous111692850
3123831098123831099TC31GENIChomozygous111692851
3123831197123831198TC34GENIChomozygous111692852
3123831463123831464TA30GENIChomozygous111692853
3123831671123831672TG12GENIChomozygous111692854
3123831925123831926GA22GENIChomozygous111692855
3123834596123834597AC42GENIChomozygous111692856
3123837266123837267CT39GENIChomozygous111692857
3123840804123840805AT4GENICheterozygous119841636