chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3100782116100782118CA--6GENICheterozygous57578629
3100783780100783784CTGG----30GENICheterozygous57578631
3100783791100783793TC--29GENICheterozygous57578633
3100783792100783793CG36GENICheterozygous57578635
3100783793100783794TTGG36GENICheterozygous57578637
3100783801100783802TG35GENICheterozygous57578639
3100783823100783824A-30GENICheterozygous58168110
3100788706100788707AAC17GENIChomozygous57578641
3100794700100794701TG25GENICheterozygous57578643
3100797333100797334TTG8GENIChomozygous57578645
3100797344100797346TG--8GENIChomozygous57578647
3100797349100797351AG--8GENIChomozygous57578649
3100799637100799638TG16GENIChomozygous57578651
3100799765100799766CG21GENIChomozygous57578653
3100799772100799773CG21GENIChomozygous57578655
3100799777100799778CT18GENIChomozygous57578657
3100799779100799780CT18GENIChomozygous57578659
3100799781100799782CG18GENIChomozygous57578661
3100799783100799784AAC18GENIChomozygous57578663
3100799786100799787CA24GENIChomozygous57578665
3100799791100799792CA24GENIChomozygous57578667
3100799799100799800TG23GENIChomozygous57578669
3100799809100799810CG24GENIChomozygous57578671
3100799815100799816TA21GENIChomozygous57932699
3100799816100799817CG21GENIChomozygous57578673
3100799818100799819CG21GENIChomozygous57578675
3100799832100799833CT29GENIChomozygous57578677
3100799841100799842CA27GENIChomozygous57578679
3100818316100818317TG16GENICheterozygous58168112