chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71204444112044442TC33GENIChomozygous115569442
71204506312045064CG28GENIChomozygous115569443
71204525212045253AG40GENIChomozygous115569444
71204557712045578AG5GENIChomozygous116246527
71204558512045586GA5GENICheterozygous115569445
71204654112046542CT24GENIChomozygous115569446
71204793712047938CG24GENIChomozygous115569447
71204929412049295CT42GENIChomozygous115569448
71205029612050297TC43GENIChomozygous115569449
71205069212050693TG26GENIChomozygous115569450
71205069312050694TA27GENIChomozygous115569451
71205126012051261CT39GENIChomozygous115569452
71205148112051482TC34GENIChomozygous115569453
71205176712051768GA25GENICheterozygous115569454
71205177112051772GA23GENICpossibly homozygous115569455
71205178712051788AG19GENICheterozygous116003690
71205223112052232GA11GENICheterozygous115569456
71205223612052237AG8GENICheterozygous115569457
71205387112053872AT28GENIChomozygous115569458
71205398712053988AG38GENIChomozygous115569459
71205444012054441GA32GENIChomozygous115569460
71205450412054505GA38GENICheterozygous115569461
71205527612055277AG27GENIChomozygous115569462
71205536412055365CT23GENIChomozygous115569463
71205580412055805CT22GENIChomozygous115569464
71205654512056546TG23GENIChomozygous115569465
71205682112056822AT37GENIChomozygous115569466
71205742512057426GA43GENIChomozygous115569467
71205876512058766AG25GENIChomozygous115569468
71205915112059152TC29GENIChomozygous115569469
71205947312059474TA14GENIChomozygous115569470
71206080012060801TC35GENIChomozygous115569471
71206162912061630AG34GENIChomozygous115569472
71206213312062134TC15GENIChomozygous115569473
71206248012062481TC19GENIChomozygous115569474