chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2224955828224955829A-7GENIChomozygous59415453
2224956843224956847TTTT----11GENICpossibly homozygous59415454
2224956844224956847TTT---11GENICheterozygous59415455
2224957415224957416CCTT25GENIChomozygous59415456
2224957780224957782TT--4GENIChomozygous59415458
2224957980224957981CCTTT9GENICheterozygous59415459
2224957980224957981CCTT9GENICheterozygous59415460
2224958080224958081CT24GENIChomozygous59415461
2224958887224958888GGTT5GENICheterozygous59775242
2224958890224958891CT7GENIChomozygous59415462
2224958897224958898CT7GENIChomozygous59415463
2224959623224959624GGCA23GENIChomozygous59415464
2224960452224960453TC6GENIChomozygous59415466
2224962375224962376GA16GENIChomozygous59415467
2224962936224962937TG6GENIChomozygous59415468
2224963178224963179AAT16GENIChomozygous59415469
2224963671224963673TT--1GENIChomozygous59775243
2224963702224963703CG12GENICheterozygous59415470
2224963746224963747AAG11GENIChomozygous59415471
2224966409224966410AAT8GENICheterozygous59938181
2224969020224969021AG11GENIChomozygous59415472
2224969399224969402TTT---14GENICheterozygous59775245
2224969400224969402TT--14GENICpossibly homozygous59415473
2224969932224969933TC17GENICheterozygous59415474
2224975339224975340AG11GENIChomozygous59415476
2224975378224975380AA--2GENIChomozygous59415477
2224976399224976400TG17GENIChomozygous59415478
2224976562224976563TA10GENIChomozygous59415479
2224977718224977719AG8GENIChomozygous59415480
2224978449224978450TA14GENIChomozygous59415481
2224979339224979340AAT8GENIChomozygous59415482
2224979629224979630GA12GENICpossibly homozygous59415483
2224972904224972905CT6GENIChomozygous60166615