chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 40341047 40341048 T C 12 GENIC homozygous 550950516 12 40341058 40341059 G A 16 GENIC homozygous 550950517 12 40341213 40341214 A C 13 GENIC homozygous 550950518 12 40341986 40341987 T - 9 GENIC homozygous 699605624 12 40342338 40342339 G A 24 GENIC homozygous 550950519 12 40342426 40342427 A G 25 GENIC homozygous 550950520 12 40342760 40342761 A G 21 GENIC homozygous 550950521 12 40349984 40349985 G GCACACACACACACACACA 7 GENIC possibly homozygous 699605627 12 40354386 40354387 G A 27 GENIC homozygous 550950522 12 40355056 40355060 GTGT ---- 7 GENIC heterozygous 699605628 12 40358199 40358200 T TC 34 GENIC homozygous 699605629 12 40358206 40358207 T TC 38 GENIC homozygous 699605630 12 40358210 40358211 G GC 39 GENIC homozygous 699605631 12 40358280 40358282 TG -- 8 GENIC heterozygous 699605633 12 40358443 40358444 C G 32 GENIC homozygous 550950523 12 40358445 40358446 C G 32 GENIC homozygous 550950524 12 40363893 40363897 GTGT ---- 5 GENIC homozygous 699605636 12 40364121 40364122 A - 5 GENIC homozygous 699605639 12 40364133 40364134 C CA 1 GENIC homozygous 699605641 12 40364774 40364775 C T 19 GENIC homozygous 550950525 12 40364782 40364783 A C 19 GENIC homozygous 550950526