chr start stop reference nuc variant nuc depth genic status zygosity variant ID 19 39272736 39272737 A G 12 GENIC homozygous 109695809 19 39280259 39280260 C T 9 GENIC homozygous 109695813 19 39280328 39280329 G A 19 GENIC homozygous 109695815 19 39280409 39280410 C A 4 GENIC homozygous 109695817 19 39280559 39280560 A G 18 GENIC homozygous 109695819 19 39281153 39281154 G C 4 GENIC homozygous 109695821 19 39284659 39284660 C T 10 GENIC homozygous 109695823 19 39284874 39284875 C A 12 GENIC homozygous 109695825 19 39285037 39285038 T C 8 GENIC homozygous 109695827 19 39285079 39285080 C T 12 GENIC homozygous 109695829 19 39285114 39285115 C A 13 GENIC homozygous 109695831 19 39285246 39285247 G T 16 GENIC homozygous 109695833 19 39285283 39285284 C T 25 GENIC homozygous 109695835 19 39286475 39286476 A G 9 GENIC homozygous 109695837 19 39287807 39287808 C T 12 GENIC heterozygous 109695839 19 39287848 39287849 C T 24 GENIC homozygous 109695841 19 39288340 39288341 T A 20 GENIC homozygous 109695843 19 39288634 39288635 A G 5 GENIC homozygous 109695845 19 39288655 39288656 T G 12 GENIC homozygous 109695847 19 39290343 39290344 A T 19 GENIC homozygous 109695849 19 39290583 39290584 C A 3 GENIC heterozygous 125287354 19 39290701 39290702 C T 17 GENIC homozygous 109695851 19 39290802 39290803 A G 20 GENIC homozygous 109695853 19 39294189 39294190 A T 16 GENIC homozygous 109926268 19 39296600 39296601 C T 18 GENIC homozygous 109695855 19 39297575 39297576 C T 15 GENIC homozygous 109695857 19 39299659 39299660 C G 19 GENIC homozygous 109695859 19 39285099 39285100 G A 14 GENIC homozygous 109781083 19 39285850 39285851 G A 6 GENIC homozygous 109781085 19 39300108 39300109 A G 16 GENIC homozygous 109781097 19 39301079 39301080 T G 10 GENIC homozygous 109695863