chr start stop reference nuc variant nuc depth genic status zygosity variant ID 14 524294 524295 T G 28 GENIC homozygous 114039976 14 524354 524355 A T 46 GENIC heterozygous 118828299 14 524731 524732 G C 29 GENIC possibly homozygous 118663188 14 525330 525331 A C 31 GENIC heterozygous 118663195 14 525447 525448 A G 31 GENIC heterozygous 118812894 14 525539 525540 G A 14 GENIC homozygous 118663198 14 525612 525613 A T 17 GENIC homozygous 118663200 14 525625 525626 T G 19 GENIC homozygous 118663202 14 525660 525661 A G 25 GENIC homozygous 118663205 14 525684 525685 G T 29 GENIC homozygous 114082266 14 525689 525690 G T 36 GENIC possibly homozygous 118663207 14 525706 525707 C A 36 GENIC possibly homozygous 118663210 14 525932 525933 T C 6 GENIC homozygous 118741761 14 526207 526208 T A 9 GENIC homozygous 118663212 14 526218 526219 C T 12 GENIC heterozygous 118812899 14 526369 526370 T C 49 GENIC heterozygous 118828300 14 526374 526375 T G 48 GENIC possibly homozygous 118663217