chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2228504640228504641TC2GENICheterozygous59427452
2228504686228504687TC14GENICpossibly homozygous59427453
2228504691228504692T-9GENIChomozygous59427454
2228505272228505273TC14GENIChomozygous59427457
2228505292228505293AAT6GENICheterozygous59427458
2228505537228505540CTC---8GENIChomozygous62338587
2228506041228506042TC24GENIChomozygous59427459
2228506325228506326TC16GENICpossibly homozygous59427462
2228506491228506492CT11GENIChomozygous59427463
2228506503228506504CT16GENICpossibly homozygous59427464
2228506548228506549CT15GENICpossibly homozygous59427465
2228506621228506622AG15GENICpossibly homozygous59427466
2228507182228507183AG21GENIChomozygous59427467
2228507496228507497CG1GENIChomozygous59427468
2228507947228507948TC4GENIChomozygous59427469
2228508507228508508TA9GENIChomozygous59427470
2228508626228508627TC13GENIChomozygous59427471
2228508825228508826GA5GENIChomozygous59427472
2228508827228508828GA5GENIChomozygous59427473
2228509048228509050CG--5GENIChomozygous60550291
2228509078228509079CT1GENIChomozygous59427477
2228509255228509256AC9GENIChomozygous59427479
2228509321228509322TA7GENIChomozygous59427480
2228509339228509340TC9GENICpossibly homozygous59427481
2228509594228509595GA13GENICpossibly homozygous59427482
2228509664228509665CT13GENICheterozygous59427483