chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
9113579406113579407TG27GENICheterozygous117803223
9113579426113579427TA24GENICheterozygous117427215
9113579428113579429CT23GENICheterozygous117427216
9113579830113579831GC83GENICheterozygous117427220
9113580153113580154AT83GENICheterozygous117427222
9113580256113580257GA67GENICheterozygous117427224
9113580265113580266GC65GENICheterozygous117427225
9113580345113580346GT26GENICheterozygous117427226
9113580355113580356AC25GENICheterozygous117427227
9113585063113585064AG38GENICheterozygous117427229
9113588131113588132GA35GENIChomozygous117645423
9113580601113580602CT29GENIChomozygous117645420
9113585167113585168CT36GENIChomozygous117645421
9113587986113587987AG28GENIChomozygous117645422
9113588230113588231CG33GENICheterozygous117803224
9113590798113590799GA27GENIChomozygous117645424
9113590838113590839GA33GENIChomozygous117645425
9113591342113591343CT21GENIChomozygous117645426
9113591817113591818CT21GENIChomozygous117645427
9113592821113592822TC20GENICpossibly homozygous117427237
9113593424113593425CA23GENIChomozygous117645428
9113594349113594350CT26GENIChomozygous117645429
9113594383113594384TC23GENIChomozygous117645430
9113596280113596281GA15GENIChomozygous117645431
9113596836113596837TC24GENIChomozygous117645432
9113597415113597416CT23GENIChomozygous117427243