chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1204754242204754243GA10GENICpossibly homozygous61063230
1204754383204754384C-26GENIChomozygous61063231
1204754838204754839CG21GENIChomozygous61063232
1204755226204755227AC19GENICpossibly homozygous61063233
1204755495204755496AT19GENIChomozygous61063234
1204756246204756247AG24GENIChomozygous61063235
1204757147204757148CT13GENICheterozygous61063236
1204758388204758389CT13GENICheterozygous61063237
1204758773204758774AACGTCCCAT3GENIChomozygous61063240
1204758869204758870CT10GENIChomozygous61063241
1204759225204759226TA15GENIChomozygous61063242
1204759233204759234TC13GENIChomozygous61063243
1204759320204759321TG19GENIChomozygous61063244