chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1274941736274941737CT13GENICheterozygous927611172
1274941969274941970CG64GENICheterozygous927611173
1274941986274941987GA71GENICheterozygous927611174
1274941989274941990CT78GENICheterozygous927611175
1274942018274942019GA85GENICheterozygous927611176
1274942061274942062GA79GENICheterozygous927611177
1274942071274942072AG76GENICheterozygous927611178
1274942092274942093GA72GENICheterozygous927611179
1274942118274942119TG64GENICheterozygous927611180
1274942169274942170TA47GENICheterozygous927611181
1274942190274942191CG42GENICheterozygous927611182
1274942193274942194AT39GENICheterozygous927611183
1274942198274942199AG35GENICheterozygous927611184
1274942208274942209AG34GENICheterozygous927611185
1274942214274942215AC32GENICheterozygous927611186
1274942220274942221TC32GENICheterozygous927611187
1274942244274942245AC30GENICheterozygous927611188