chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 50503225 50503226 G A 36 GENIC homozygous 114340603 13 50503539 50503540 G A 49 GENIC homozygous 114340605 13 50503592 50503593 C T 42 GENIC homozygous 114340607 13 50503859 50503860 G A 47 GENIC homozygous 114340609 13 50504347 50504348 T C 41 GENIC homozygous 114340611 13 50504459 50504460 T C 34 GENIC homozygous 114340613 13 50504767 50504768 G A 48 GENIC homozygous 114340615 13 50505533 50505534 C T 46 GENIC homozygous 114340617 13 50505720 50505721 T C 46 GENIC homozygous 114340619 13 50505769 50505770 T C 48 GENIC homozygous 114340621 13 50505841 50505842 G C 39 GENIC homozygous 114340623 13 50505888 50505889 T C 30 GENIC homozygous 114340624 13 50506251 50506252 A G 36 GENIC homozygous 114340626 13 50506355 50506356 A G 38 GENIC homozygous 114340628 13 50506492 50506493 C T 45 GENIC homozygous 114340630 13 50508870 50508871 C T 43 GENIC homozygous 114340632 13 50508941 50508942 T C 55 GENIC homozygous 114340634 13 50509004 50509005 G C 47 GENIC homozygous 114340636 13 50509363 50509364 C T 36 GENIC homozygous 114340638 13 50509504 50509505 A C 17 GENIC homozygous 118498344 13 50509748 50509749 T C 59 GENIC homozygous 114340640 13 50510138 50510139 C T 57 GENIC homozygous 114340642 13 50510397 50510398 T G 38 GENIC homozygous 114340644 13 50505501 50505502 G 38 GENIC homozygous 129052761 13 50509507 50509507 ACCC 17 GENIC homozygous 129052762 13 50509551 50509552 A 22 GENIC homozygous 129052763 13 50509431 50509432 G A 22 GENIC possibly homozygous 114549956 13 50512198 50512199 C T 10 GENIC heterozygous 118498347 13 50513078 50513081 CCA 39 GENIC possibly homozygous 129052765