chr start stop reference nuc variant nuc depth genic status zygosity variant ID 6 3518560 3518561 G A 23 GENIC homozygous 975817591 6 3518573 3518574 T C 21 GENIC homozygous 975817592 6 3518576 3518577 T G 20 GENIC homozygous 975817593 6 3519281 3519282 T C 18 GENIC homozygous 975817594 6 3519657 3519658 A G 31 GENIC homozygous 975817595 6 3519689 3519690 G C 32 GENIC homozygous 975817596 6 3519846 3519847 T C 20 GENIC homozygous 975817597 6 3519913 3519914 C T 23 GENIC possibly homozygous 975817598 6 3520993 3520994 T C 20 GENIC homozygous 975817599 6 3521222 3521223 G A 27 GENIC homozygous 975817600 6 3521476 3521477 T C 18 GENIC homozygous 975817601 6 3521550 3521551 C T 19 GENIC homozygous 975817602 6 3521587 3521588 T C 22 GENIC homozygous 975817603 6 3521990 3521991 T C 15 GENIC homozygous 975817604 6 3522071 3522072 A G 16 GENIC possibly homozygous 975817605 6 3522172 3522173 A C 31 GENIC homozygous 975817606 6 3522247 3522248 T C 19 GENIC homozygous 975817607 6 3522413 3522414 T A 16 GENIC homozygous 975817608