chr start stop reference nuc variant nuc depth genic status zygosity variant ID 6 3518560 3518561 G A 41 GENIC homozygous 979146382 6 3518573 3518574 T C 43 GENIC homozygous 979146383 6 3518576 3518577 T G 44 GENIC homozygous 979146384 6 3519281 3519282 T C 14 GENIC homozygous 979146385 6 3519657 3519658 A G 29 GENIC possibly homozygous 979146386 6 3519689 3519690 G C 32 GENIC homozygous 979146387 6 3519846 3519847 T C 21 GENIC homozygous 979146388 6 3519913 3519914 C T 17 GENIC homozygous 979146389 6 3520993 3520994 T C 67 GENIC homozygous 979146390 6 3521222 3521223 G A 34 GENIC homozygous 979146391 6 3521476 3521477 T C 47 GENIC homozygous 979146392 6 3521550 3521551 C T 53 GENIC homozygous 979146393 6 3521587 3521588 T C 44 GENIC homozygous 979146394 6 3521990 3521991 T C 42 GENIC homozygous 979146395 6 3522071 3522072 A G 56 GENIC homozygous 979146396 6 3522172 3522173 A C 36 GENIC homozygous 979146397 6 3522247 3522248 T C 39 GENIC homozygous 979146398 6 3522413 3522414 T A 66 GENIC homozygous 979146399