chr start stop reference nuc variant nuc depth genic status zygosity variant ID 8 36401932 36401933 C T 31 GENIC homozygous 116456504 8 36402338 36402339 G C 16 GENIC homozygous 116456505 8 36402406 36402407 G C 27 GENIC homozygous 116456506 8 36402751 36402752 C T 24 GENIC possibly homozygous 116456507 8 36403452 36403453 A T 29 GENIC homozygous 116456508 8 36403511 36403512 T C 34 GENIC homozygous 116456509 8 36403623 36403624 T C 28 GENIC homozygous 116456510 8 36403990 36403991 C T 24 GENIC homozygous 116456511 8 36404313 36404314 G A 29 GENIC homozygous 116456512 8 36404417 36404418 T C 25 GENIC homozygous 116456513 8 36404616 36404617 A G 48 GENIC homozygous 116456514 8 36405581 36405582 G A 28 GENIC homozygous 116456515 8 36405731 36405732 G A 34 GENIC homozygous 116456516 8 36405820 36405821 T C 25 GENIC homozygous 116456517 8 36405845 36405846 A G 29 GENIC homozygous 116456518 8 36406520 36406521 G T 41 GENIC homozygous 116456519 8 36406897 36406898 G A 27 GENIC homozygous 116456520 8 36407524 36407525 G A 26 GENIC homozygous 116456521 8 36407593 36407594 G A 26 GENIC homozygous 116456522 8 36407941 36407942 A G 9 GENIC homozygous 116456523 8 36408579 36408580 G A 28 GENIC homozygous 116456524 8 36409030 36409031 G A 23 GENIC homozygous 116456525 8 36409673 36409674 C T 41 GENIC homozygous 116456526 8 36409923 36409924 C T 14 GENIC homozygous 116456528 8 36409968 36409969 C T 16 GENIC homozygous 116456529 8 36410330 36410331 G T 38 GENIC homozygous 116456530