chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1798570569857057AC82GENICheterozygous782670012
1798570879857088GT74GENICheterozygous782670013
1799251289925129GA103GENICheterozygous782670014
1799251929925193AG140GENICheterozygous782670015
1799251959925196GT141GENICheterozygous782670016
1799251979925198TC145GENICheterozygous782670017
1799252269925227CG144GENICheterozygous782670018
1799252439925244AG133GENICheterozygous782670019
1799253459925346TC76GENICheterozygous782670020
1799253899925390CT114GENICheterozygous782670021
1799254399925440AT143GENICheterozygous782670022
1799254469925447TA137GENICheterozygous782670023
1799254819925482TC126GENICheterozygous782670024
1799255889925589TA29GENICheterozygous782670025
1799256069925607GT36GENICheterozygous782670026
1799256159925616GA35GENICheterozygous782670027
1799256229925623CT36GENICheterozygous782670028
1799266399926640GA52GENIChomozygous782670029
1799268609926861GC44GENIChomozygous782670030
1799301869930187TG63GENIChomozygous782670031
1799334969933497TG55GENIChomozygous782670032