chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1182386348182386348CTT30GENIChomozygous135449320
1182386856182386857GT25GENIChomozygous135764411
1182387081182387082TC28GENIChomozygous135764412
1182387451182387452TG27GENIChomozygous135764413
1182389736182389737CA28GENICpossibly homozygous153898811
1182389736182389737C28GENICheterozygous402974966
1182391441182391442TC28GENIChomozygous135764414
1182392459182392460CT23GENIChomozygous135764415
1182393957182393958TA20GENIChomozygous135764416
1182394471182394472T17GENIChomozygous135449321
1182394491182394492A11GENIChomozygous135449322
1182395076182395077GA26GENIChomozygous135764417
1182398577182398578CT25GENIChomozygous135764418
1182400797182400798TC12GENIChomozygous135764419
1182401413182401413AGAT26GENIChomozygous135449323
1182402539182402540CT14GENIChomozygous135764424
1182402584182402585T15GENIChomozygous135449324
1182402611182402611AT12GENIChomozygous135449325
1182403564182403565GA19GENIChomozygous135764425
1182404716182404717AC28GENIChomozygous135764426
1182405272182405273GA24GENIChomozygous135764427
1182406099182406100TC23GENIChomozygous135764428
1182409830182409831TC28GENIChomozygous135764429
1182409918182409919CT25GENIChomozygous135764430