chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1124772983124772984AG45GENIChomozygous108214264
1124773235124773236CT52GENIChomozygous108214265
1124773789124773790TC61GENIChomozygous108214266
1124774531124774532CT40GENIChomozygous108214267
1124774868124774869AG26GENIChomozygous108214268
1124775951124775952AC61GENIChomozygous108214269
1124776292124776293CG38GENIChomozygous108214270
1124777324124777325AC60GENIChomozygous108214271
1124777682124777683TG50GENIChomozygous108214272
1124778303124778304AG49GENIChomozygous108214273
1124779524124779525CT71GENIChomozygous108214274
1124780177124780178TC44GENIChomozygous108214275
1124783133124783134AC33GENIChomozygous108214276
1124784336124784337GA63GENIChomozygous108214277
1124784887124784888TC55GENIChomozygous108214278
1124785613124785614CA52GENIChomozygous108214279
1124785670124785671GA48GENIChomozygous108214280
1124785683124785684CA49GENIChomozygous108214281
1124785039124785040CT16GENIChomozygous127555214
1124785783124785811GAGGTGGCTCCTGGGAGGTGGCTCCTGG44GENIChomozygous127424732
1124785833124785834GA46GENIChomozygous108214282
1124786425124786425A12GENIChomozygous127424733
1124786209124786210TA32GENICheterozygous131791982
1124793084124793085AT51GENIChomozygous108214283
1124793269124793270GA32GENIChomozygous108214284
1124795862124795863G31GENIChomozygous127424734
1124795899124795900A37GENIChomozygous127424735