chr start stop reference nuc variant nuc depth genic status zygosity variant ID 4 161446528 161446529 G A 15 GENIC homozygous 71276356 4 161446855 161446856 C G 5 GENIC homozygous 71276358 4 161446863 161446864 C T 5 GENIC homozygous 71276360 4 161448673 161448674 C A 4 GENIC homozygous 71276364 4 161449928 161449929 C T 7 GENIC homozygous 71276388 4 161450642 161450643 A C 19 GENIC homozygous 71276392 4 161450915 161450916 A G 31 GENIC homozygous 71276394 4 161451267 161451268 C T 13 GENIC homozygous 71276396 4 161451824 161451825 A G 19 GENIC homozygous 71276398 4 161452668 161452669 C T 21 GENIC homozygous 71276400 4 161452791 161452792 T C 22 GENIC homozygous 71276402 4 161453638 161453639 T C 17 GENIC homozygous 71276404 4 161453675 161453676 C T 33 GENIC homozygous 71276406 4 161454044 161454045 A G 12 GENIC homozygous 71276408 4 161454481 161454482 T C 18 GENIC homozygous 71276412 4 161454956 161454957 G A 28 GENIC homozygous 71276413 4 161455267 161455268 G A 13 GENIC homozygous 71276415 4 161456045 161456046 C G 7 GENIC homozygous 71276427 4 161456782 161456783 G A 26 GENIC possibly homozygous 71276429 4 161457019 161457020 G A 10 GENIC homozygous 71276431 4 161457528 161457529 C T 29 GENIC homozygous 71276433 4 161459693 161459694 C T 21 GENIC homozygous 71276435 4 161460513 161460514 T C 29 GENIC heterozygous 71276437 4 161460619 161460620 C T 9 GENIC homozygous 71276439 4 161463155 161463156 T G 19 GENIC homozygous 71276441 4 161463525 161463526 A G 23 GENIC homozygous 71276443 4 161464184 161464185 A G 9 GENIC homozygous 72716120