chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
9114116186114116187TC14GENICheterozygous126533299
9114116845114116846GA10GENIChomozygous117428624
9114117064114117065CG21GENIChomozygous117428628
9114118301114118302TC13GENICheterozygous126533301
9114118302114118303GT13GENICheterozygous126533303
9114118326114118327CG14GENICheterozygous126533305
9114118539114118540TC17GENICheterozygous126533307
9114118604114118605CT15GENICheterozygous126533309
9114118615114118616CT13GENICheterozygous126533311
9114118652114118653AG17GENICheterozygous126533313
9114118679114118680CT18GENICheterozygous126533315
9114118921114118922TG33GENIChomozygous126533317
9114119036114119037CT20GENICheterozygous126533319
9114119101114119102AC14GENICheterozygous126533321
9114120102114120103GC18GENIChomozygous126533323
9114120564114120565CT12GENICheterozygous126533325
9114122543114122544CT7GENIChomozygous117645940
9114122544114122545CG7GENIChomozygous117645941
9114128906114128907CT20GENIChomozygous117645943
9114129927114129928AG23GENIChomozygous117645944
9114130744114130745GA15GENIChomozygous117428692
9114131066114131067CT14GENIChomozygous117645945
9114131224114131225AG6GENIChomozygous117645946
9114131225114131226GA6GENIChomozygous117645947
9114131237114131238CT14GENIChomozygous117645948
9114131282114131283GA17GENIChomozygous117645949
9114131307114131308GA23GENIChomozygous117645950
9114131946114131947GA27GENIChomozygous117645951
9114132115114132116GC8GENIChomozygous117645952
9114132123114132124GA13GENIChomozygous117645953
9114132146114132147GC20GENIChomozygous117645954
9114132979114132980AG17GENIChomozygous117645955
9114133724114133725CT13GENIChomozygous117428703