chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1141732195141732196AC74INTERGENICheterozygous74485127
1141732544141732545AT60INTERGENICheterozygous74485131
1141732725141732726AG26INTERGENIChomozygous74485133
1141732726141732727GT26INTERGENIChomozygous74485135
1141732778141732779AT18INTERGENICheterozygous74485137
1141771122141771123CA74INTERGENICheterozygous74485157
1141771161141771162CG77INTERGENICheterozygous74485159
1141771185141771186TC76INTERGENICheterozygous74485161
1141772777141772778AT15INTERGENIChomozygous75595705
1141772824141772825AT16INTERGENICheterozygous75784855
1141773907141773908CA39INTERGENICheterozygous74485187
1141774897141774898CG16INTERGENIChomozygous75137183
1141791048141791049CT9INTERGENICpossibly homozygous78122601
1141791057141791058GA10INTERGENIChomozygous75595708
1141791178141791179CG31INTERGENICheterozygous75137184
1141791400141791401CT16INTERGENICpossibly homozygous74485223
1141791480141791481TG47INTERGENICheterozygous74485225
1141791596141791597TG8INTERGENIChomozygous74485229
1141791637141791638GC6INTERGENICheterozygous74485231
1141791737141791738TA10INTERGENICpossibly homozygous74485233
1141791743141791744GT9INTERGENIChomozygous74485235
1141791852141791853CT25INTERGENICheterozygous74485237
1141791874141791875GA20INTERGENICpossibly homozygous74485239
1141773953141773954CT31INTERGENICheterozygous75871867