chr start stop reference nuc variant nuc depth genic status zygosity variant ID 8 2684749 2684750 T - 6 GENIC homozygous 695863593 8 2684764 2684765 G - 6 GENIC homozygous 695863594 8 2684837 2684838 G GA 4 GENIC homozygous 695863595 8 2684898 2684899 T A 8 GENIC homozygous 537016837 8 2684911 2684912 G A 10 GENIC homozygous 537016838 8 2686349 2686350 T - 39 GENIC heterozygous 695863596 8 2691610 2691611 C - 17 GENIC homozygous 695863597 8 2691861 2691862 A AT 11 GENIC homozygous 695863598 8 2692114 2692115 G T 79 GENIC heterozygous 537016839 8 2692157 2692158 C G 76 GENIC heterozygous 534667090 8 2692177 2692178 A C 77 GENIC heterozygous 537016840 8 2692219 2692220 T A 89 GENIC heterozygous 537016841 8 2692231 2692232 T - 63 GENIC heterozygous 695863599 8 2692241 2692242 C G 82 GENIC heterozygous 537016842 8 2692280 2692281 C A 76 GENIC heterozygous 537016843 8 2693245 2693246 A T 70 GENIC heterozygous 537016844 8 2693252 2693253 G A 73 GENIC heterozygous 537016845 8 2693639 2693640 G T 15 GENIC possibly homozygous 534667091 8 2693667 2693668 G T 13 GENIC heterozygous 537016846 8 2693669 2693670 G T 13 GENIC heterozygous 537016847 8 2696284 2696285 A T 23 GENIC homozygous 537016848 8 2696360 2696361 C T 13 GENIC homozygous 537016849 8 2700102 2700103 G GA 12 GENIC homozygous 695863600 8 2700114 2700115 A AC 12 GENIC homozygous 695863601 8 2700277 2700278 C CT 15 GENIC homozygous 695863602 8 2700282 2700283 T - 13 GENIC homozygous 695863603