chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1182386348182386348CTT13GENIChomozygous135449320
1182386856182386857GT21GENIChomozygous135764411
1182387081182387082TC15GENIChomozygous135764412
1182387451182387452TG21GENIChomozygous135764413
1182391441182391442TC12GENIChomozygous135764414
1182392459182392460CT17GENIChomozygous135764415
1182394471182394472T13GENIChomozygous135449321
1182394491182394492A12GENIChomozygous135449322
1182400797182400798TC8GENIChomozygous135764419
1182389736182389737CA26GENIChomozygous153898811
1182389736182389737C26GENICheterozygous402974966
1182393957182393958TA7GENIChomozygous135764416
1182395076182395077GA15GENIChomozygous135764417
1182398577182398578CT16GENIChomozygous135764418
1182401413182401413AGAT8GENIChomozygous135449323
1182402539182402540CT13GENIChomozygous135764424
1182402584182402585T11GENIChomozygous135449324
1182402611182402611AT11GENIChomozygous135449325
1182403564182403565GA12GENIChomozygous135764425
1182404716182404717AC9GENIChomozygous135764426
1182405272182405273GA11GENICpossibly homozygous135764427
1182406099182406100TC15GENIChomozygous135764428
1182409830182409831TC10GENIChomozygous135764429
1182409918182409919CT14GENIChomozygous135764430