chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 52127275 52127276 C T 28 GENIC homozygous 114345467 13 52127277 52127278 G A 30 GENIC homozygous 114345469 13 52127577 52127578 C A 9 GENIC homozygous 115024935 13 52127603 52127604 T C 11 GENIC homozygous 114672475 13 52128147 52128148 G A 23 GENIC homozygous 114345471 13 52128827 52128828 C A 22 GENIC possibly homozygous 114345473 13 52129299 52129300 G A 29 GENIC homozygous 114345475 13 52129311 52129312 G A 30 GENIC homozygous 114345477 13 52129415 52129416 G A 14 GENIC homozygous 114720455 13 52130147 52130148 A C 12 GENIC possibly homozygous 114672477 13 52131681 52131682 C T 22 GENIC homozygous 114672478 13 52131792 52131793 T C 18 GENIC homozygous 114345479 13 52131981 52131982 G A 18 GENIC homozygous 114345481 13 52132650 52132651 A C 17 GENIC homozygous 114345483 13 52132740 52132741 A G 13 GENIC homozygous 114857687 13 52132994 52132995 C T 18 GENIC homozygous 114345485 13 52134365 52134366 C T 20 GENIC homozygous 114345487 13 52135947 52135948 T C 35 GENIC homozygous 114345489