chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 40248280 40248281 C G 8 GENIC homozygous 877841526 10 40248287 40248288 A G 9 GENIC homozygous 877841527 10 40248300 40248301 C T 5 GENIC homozygous 877841528 10 40248480 40248481 C A 15 GENIC homozygous 877841529 10 40248587 40248588 C G 10 GENIC homozygous 877841530 10 40248638 40248639 C T 4 GENIC homozygous 877841531 10 40248938 40248939 T C 6 GENIC homozygous 877841532 10 40249700 40249701 T C 9 GENIC heterozygous 877841533 10 40249947 40249948 T G 9 GENIC homozygous 877841534 10 40251240 40251241 G A 9 GENIC homozygous 877841535 10 40251529 40251530 T C 14 GENIC homozygous 877841536 10 40251563 40251564 G C 15 GENIC homozygous 877841537 10 40251735 40251736 A G 13 GENIC homozygous 877841538 10 40252051 40252052 C T 9 GENIC homozygous 877841539 10 40252934 40252935 T C 13 GENIC homozygous 877841540 10 40253450 40253451 C T 12 GENIC homozygous 877841541 10 40253751 40253752 T C 13 GENIC homozygous 877841542 10 40253991 40253992 T C 16 GENIC homozygous 877841543 10 40254191 40254192 A C 5 GENIC homozygous 877841544 10 40254347 40254348 A G 12 GENIC homozygous 877841545 10 40254376 40254377 G A 8 GENIC homozygous 877841546 10 40254433 40254434 A G 4 GENIC homozygous 877841547 10 40254993 40254994 G A 16 GENIC homozygous 877841548