chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 65824182 65824183 G A 42 GENIC homozygous 51478384 10 65824701 65824702 T C 42 GENIC homozygous 51478385 10 65825360 65825361 T G 30 GENIC homozygous 51478386 10 65825587 65825588 T C 23 GENIC homozygous 51478387 10 65825782 65825783 C T 44 GENIC homozygous 51478388 10 65826041 65826042 G C 48 GENIC homozygous 51478389 10 65826275 65826276 T C 39 GENIC homozygous 51478390 10 65826464 65826465 G GTGA 49 GENIC homozygous 51478391 10 65826710 65826711 A AT 8 GENIC heterozygous 51478392 10 65826710 65826711 A ATT 8 GENIC heterozygous 51478393 10 65827625 65827626 T C 26 GENIC homozygous 51478394 10 65827927 65827929 AA -- 48 GENIC homozygous 51478395 10 65828976 65828977 T C 36 GENIC homozygous 51478398 10 65829659 65829660 A G 27 GENIC homozygous 51478399 10 65829745 65829746 G A 17 GENIC homozygous 51478400 10 65829803 65829804 G GCCTAGCAAGCGCAAGGC 21 GENIC homozygous 51478401 10 65830492 65830493 G C 33 GENIC homozygous 51478402 10 65831157 65831158 T C 41 GENIC homozygous 51478403 10 65831708 65831709 T C 55 GENIC homozygous 51478404 10 65832036 65832037 T G 55 GENIC homozygous 51478405 10 65832071 65832072 G - 42 GENIC homozygous 51478406