chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 26322686 26322687 A T 8 GENIC homozygous 50147542 12 26323265 26323266 G - 6 GENIC heterozygous 50147548 12 26323613 26323614 C T 23 GENIC possibly homozygous 50485094 12 26323970 26323971 T C 22 GENIC homozygous 50147550 12 26324285 26324286 C T 14 GENIC possibly homozygous 50147552 12 26324307 26324308 C T 18 GENIC heterozygous 50405082 12 26325403 26325404 C G 24 GENIC homozygous 50147554 12 26326225 26326226 T C 4 GENIC homozygous 50147558 12 26326358 26326359 T A 18 GENIC homozygous 50405086 12 26326415 26326416 A G 13 GENIC heterozygous 50147560 12 26326618 26326619 C A 15 GENIC possibly homozygous 50485096 12 26326905 26326906 A C 19 GENIC possibly homozygous 50147562 12 26328596 26328597 G T 20 GENIC possibly homozygous 50147564 12 26329440 26329441 T C 11 GENIC homozygous 50147566 12 26329636 26329637 T - 2 GENIC homozygous 50539333 12 26330598 26330599 C T 15 GENIC possibly homozygous 50405090 12 26333171 26333172 C T 2 GENIC heterozygous 50147570 12 26333453 26333454 G A 10 GENIC heterozygous 50147572 12 26333616 26333617 C A 17 GENIC homozygous 50405092 12 26334167 26334168 T C 6 GENIC heterozygous 50147576 12 26334825 26334826 C A 6 GENIC homozygous 50147578 12 26336017 26336018 T TACAC 3 GENIC heterozygous 50147580 12 26337339 26337340 A AGCCT 1 GENIC homozygous 50485098