chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2174552617174552618AG65GENIChomozygous136373306
2174554627174554628AG72GENIChomozygous136373307
2174557430174557431AT21GENICpossibly homozygous141422401
2174557433174557434AT26GENIChomozygous136373308
2174557453174557454GA21GENICpossibly homozygous154018974
2174557465174557466AG36GENIChomozygous154018975
2174559635174559636AG44GENIChomozygous136373309
2174559652174559653CG44GENICpossibly homozygous154018979
2174559656174559657CG44GENICpossibly homozygous154018981
2174557453174557454G21GENICheterozygous403028003
2174559639174559641AG44GENIChomozygous135961219
2174557465174557466A36GENICheterozygous403028004
2174559652174559653C44GENICheterozygous403028005
2174559656174559657C44GENICheterozygous403028007
2174559660174559661CG44GENICpossibly homozygous154018983
2174559660174559661C44GENICheterozygous403028009
2174560693174560694TC48GENIChomozygous136373310
2174561613174561614T63GENICpossibly homozygous141135572
2174562661174562662GA49GENIChomozygous136373311
2174563605174563607CA47GENIChomozygous135961220
2174567329174567330CT49GENIChomozygous136373312