chr start stop reference nuc variant nuc depth genic status zygosity variant ID 4 133995812 133995813 T C 31 GENIC homozygous 71151434 4 133995934 133995935 G A 39 GENIC homozygous 71151437 4 133995982 133995983 C T 23 GENIC homozygous 71151440 4 133996073 133996074 T C 38 GENIC homozygous 71151443 4 133996166 133996167 A G 24 GENIC homozygous 71151447 4 133996323 133996324 C T 20 GENIC homozygous 71151450 4 133996637 133996638 T C 38 GENIC homozygous 71151457 4 133997177 133997178 A C 33 GENIC homozygous 71151458 4 133997365 133997366 C T 29 GENIC homozygous 71151461 4 133997750 133997751 T G 26 GENIC homozygous 71151467 4 133997922 133997923 C T 46 GENIC homozygous 71151470 4 133997988 133997989 G A 39 GENIC homozygous 71622546 4 133998138 133998139 C A 25 GENIC homozygous 71151473 4 133998188 133998189 A T 25 GENIC homozygous 71151476 4 133998461 133998462 T C 38 GENIC homozygous 71151479 4 133998609 133998610 T C 26 GENIC homozygous 71151482 4 133998646 133998647 C T 23 GENIC homozygous 71151485 4 133998648 133998649 G A 26 GENIC homozygous 71151488 4 133998681 133998682 G A 29 GENIC homozygous 71151491 4 133998692 133998693 T C 30 GENIC homozygous 71151494 4 133998742 133998743 G C 24 GENIC homozygous 71151497 4 133998818 133998819 A G 31 GENIC homozygous 71151503 4 133998917 133998918 A C 27 GENIC homozygous 71151506 4 133998994 133998995 T C 21 GENIC homozygous 71151509 4 133999440 133999441 C T 20 GENIC homozygous 71151512 4 133999338 133999339 C A 21 GENIC heterozygous 73915054 4 133999336 133999337 C A 19 GENIC heterozygous 73915051