chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
39297076592970765G2GENIChomozygous127909148
39297082492970825A8GENIChomozygous127909149
39297089292970893A12GENIChomozygous127909150
39297092092970921A11GENIChomozygous127909151
39297098892970989A9GENIChomozygous127909152
39297101392971013A9GENIChomozygous127909153
39297106192971062C8GENIChomozygous127909154
39297112192971122C10GENIChomozygous127909155
39297120192971203CC6GENIChomozygous127909156
39297123192971232T4GENIChomozygous127909157
39297123992971240G5GENIChomozygous127909158
39297125092971250T5GENIChomozygous127909159
39297126292971263AT4GENIChomozygous121836651
39297126392971264TA3GENIChomozygous121836652
39297126792971267AC3GENIChomozygous127909160
39297127292971273T3GENIChomozygous127909161
39297127592971276C3GENIChomozygous127909162
39297134192971342C5GENIChomozygous127909163
39297135292971353T5GENIChomozygous127909164
39297140992971409T2GENIChomozygous127909165
39297141592971416A2GENIChomozygous127909166
39297142092971421T2GENIChomozygous127909167
39297142392971424C2GENIChomozygous127909168
39297144792971448G1GENIChomozygous127909169
39297159092971591G2GENIChomozygous127909176
39297160592971606G3GENIChomozygous127909177
39297160892971608A3GENIChomozygous127909178
39297161692971617G3GENIChomozygous127909179
39297163092971631CG3GENIChomozygous121836668
39297163092971630T3GENIChomozygous127909180
39297167092971671C7GENIChomozygous127909181
39297168692971686T7GENIChomozygous127909182
39297170692971706A7GENIChomozygous127909183
39297171392971714C7GENIChomozygous127909184
39297171592971716TA7GENIChomozygous127985633
39297172092971720T6GENIChomozygous127909185
39297172392971725TA6GENIChomozygous127909186
39297173892971738A4GENIChomozygous127909187
39297175292971753G3GENIChomozygous127909188
39297185292971852AA5GENIChomozygous127909189
39297185592971855C4GENIChomozygous127909190