chr start stop reference nuc variant nuc depth genic status zygosity variant ID 20 5021111 5021112 T C 26 GENIC homozygous 109076133 20 5021161 5021162 A G 21 GENIC homozygous 109076135 20 5021176 5021177 G A 17 GENIC homozygous 109076137 20 5022247 5022248 G A 26 GENIC homozygous 109076138 20 5023844 5023845 A G 23 GENIC homozygous 109076140 20 5024202 5024203 C T 13 GENIC homozygous 109076142 20 5024403 5024404 A G 27 GENIC homozygous 109076149 20 5025912 5025913 G A 23 GENIC homozygous 109076157 20 5026382 5026383 C T 31 GENIC homozygous 109076161 20 5026697 5026698 G C 24 GENIC homozygous 109076163 20 5027340 5027341 C T 40 GENIC homozygous 109076165 20 5027891 5027892 T C 29 GENIC homozygous 109076167 20 5028315 5028316 T C 32 GENIC homozygous 109076169 20 5029920 5029921 A G 32 GENIC homozygous 109296678 20 5030110 5030111 T C 31 GENIC homozygous 109296682 20 5030785 5030786 A G 34 GENIC homozygous 109296686 20 5032612 5032613 C T 37 GENIC homozygous 109390148 20 5030909 5030910 G T 30 GENIC homozygous 109390145 20 5031374 5031375 T C 32 GENIC homozygous 109390146 20 5032592 5032593 G A 32 GENIC homozygous 109390147 20 5034930 5034931 T G 34 GENIC homozygous 109390149