chr start stop reference nuc variant nuc depth genic status zygosity variant ID 4 9516601 9516602 T C 37 GENIC homozygous 112490272 4 9516669 9516670 C T 40 GENIC homozygous 112490274 4 9516862 9516863 T C 42 GENIC homozygous 112490276 4 9516951 9516952 T C 28 GENIC homozygous 112490277 4 9516984 9516985 G A 31 GENIC homozygous 112490279 4 9517044 9517045 T C 35 GENIC homozygous 112490281 4 9517134 9517135 T C 51 GENIC heterozygous 112490283 4 9517167 9517168 A G 54 GENIC heterozygous 112490285 4 9517171 9517172 G A 56 GENIC heterozygous 112490287 4 9517184 9517185 C A 59 GENIC heterozygous 112490289 4 9517186 9517187 C G 57 GENIC heterozygous 112996756 4 9517241 9517242 T C 49 GENIC heterozygous 112490291 4 9517294 9517295 A C 39 GENIC homozygous 112490293