chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1115461536115461537T-12GENICheterozygous61671318
1115466490115466491A-5GENICheterozygous60809089
1115476396115476398TG--2GENICheterozygous62350618
1115487652115487655CCC---9GENICheterozygous62312004
1115490889115490891TC--17GENICheterozygous62152472
1115494122115494123CCT2GENICheterozygous62152476
1115499962115499963CCAA3GENICheterozygous62152480
1115506006115506007AATC7GENICheterozygous61505539
1115507488115507489T-12GENIChomozygous60809120
1115507526115507527GT9GENIChomozygous60809121
1115507547115507548AT6GENIChomozygous61300781
1115507549115507550GGT7GENIChomozygous62152488
1115509311115509312T-3GENICheterozygous61671320
1115521483115521484AAAT1GENIChomozygous60809140
1115531481115531482T-4GENICheterozygous60809174
1115532361115532362T-7GENICheterozygous60809179
1115546813115546814T-13GENIChomozygous60809185
1115558966115558967TTC11GENICheterozygous60809190
1115564984115564985AG15GENIChomozygous60809197
1115574512115574514TG--9GENICheterozygous62350620
1115574924115574925CCAA3GENICheterozygous61671323
1115580462115580463C-7GENIChomozygous60809223
1115589357115589362GGGTC-----11GENICheterozygous60809234
1115593455115593460TCGGG-----23GENIChomozygous60809243
1115600671115600672TTACTTTG1GENIChomozygous62230456
1115616920115616921CCT10GENIChomozygous60809296
1115616927115616928CCA12GENIChomozygous60809297
1115629571115629573GT--15GENICheterozygous62152540
1115630889115630890GGCA28GENIChomozygous60809320
1115632362115632363TTACACAC6GENICheterozygous62266467
1115634334115634335AAT11GENICheterozygous60809327
1115634335115634336T-11GENICheterozygous62266468
1115646161115646162T-6GENICheterozygous60809349