chr start stop reference nuc variant nuc depth genic status zygosity variant ID 11 31719916 31719917 C T 28 GENIC homozygous 799834409 11 31720869 31720870 A G 28 GENIC homozygous 799834410 11 31721277 31721278 G A 34 GENIC homozygous 799834411 11 31722705 31722706 T A 26 GENIC homozygous 799834412 11 31723011 31723012 C T 36 GENIC homozygous 799834413 11 31723854 31723855 G A 35 GENIC homozygous 799834414 11 31724160 31724161 C G 25 GENIC homozygous 799834415 11 31724703 31724704 A C 33 GENIC homozygous 799834416 11 31728249 31728250 C A 24 GENIC homozygous 799834417 11 31731036 31731037 C T 33 GENIC homozygous 799834418 11 31731759 31731760 A G 41 GENIC heterozygous 799834419 11 31731763 31731764 A G 41 GENIC heterozygous 799834420 11 31732574 31732575 C T 30 GENIC homozygous 799834421 11 31732769 31732770 T C 32 GENIC homozygous 799834422 11 31732799 31732800 A G 35 GENIC homozygous 799834423 11 31734460 31734461 A G 30 GENIC homozygous 799834424 11 31736309 31736310 G A 50 GENIC homozygous 799834425 11 31736800 31736801 T C 31 GENIC homozygous 799834426 11 31737948 31737949 A G 39 GENIC possibly homozygous 799834427 11 31738577 31738578 C T 29 GENIC homozygous 799834428 11 31740031 31740032 T C 55 GENIC heterozygous 799834429 11 31740577 31740578 G A 30 GENIC homozygous 799834430 11 31741852 31741853 G A 40 GENIC homozygous 799834431 11 31742695 31742696 T C 27 GENIC possibly homozygous 799834432 11 31743622 31743623 A T 32 GENIC homozygous 799834433 11 31743917 31743918 G A 31 GENIC homozygous 799834434 11 31745524 31745525 C T 22 GENIC homozygous 799834435 11 31746642 31746643 C G 27 GENIC homozygous 799834436 11 31747409 31747410 A T 33 GENIC possibly homozygous 799834437 11 31749282 31749283 A T 36 GENIC homozygous 799834438 11 31749631 31749632 G A 40 GENIC homozygous 799834439 11 31749841 31749842 T C 41 GENIC homozygous 799834440 11 31750179 31750180 G A 28 GENIC homozygous 799834441 11 31750722 31750723 A G 38 GENIC homozygous 799834442