chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 43752852 43752853 G A 32 GENIC homozygous 116766698 10 43753508 43753509 A G 33 GENIC homozygous 116766700 10 43754526 43754527 C T 43 GENIC homozygous 117128470 10 43755495 43755496 C G 17 GENIC homozygous 116766702 10 43755659 43755660 C T 20 GENIC homozygous 116766706 10 43756583 43756584 A G 3 GENIC homozygous 116579496 10 43757195 43757196 C T 30 GENIC homozygous 117128472 10 43757648 43757649 A G 20 GENIC homozygous 116766710 10 43758233 43758234 C T 30 GENIC homozygous 116766712 10 43759470 43759471 A T 18 GENIC homozygous 116766714 10 43760186 43760187 T C 27 GENIC homozygous 116766716 10 43760278 43760279 A T 28 GENIC homozygous 116766718 10 43760760 43760761 C A 27 GENIC homozygous 116766720 10 43761579 43761580 T C 21 GENIC homozygous 116766722 10 43761930 43761931 C T 40 GENIC homozygous 116766724 10 43763430 43763431 C T 11 GENIC homozygous 116766726 10 43764992 43764993 T C 24 GENIC homozygous 116766728 10 43765475 43765476 C A 16 GENIC homozygous 116766730 10 43767001 43767002 G A 12 GENIC homozygous 116766732 10 43767272 43767273 T A 13 GENIC homozygous 116766734 10 43767402 43767403 G C 21 GENIC homozygous 116766736 10 43767468 43767469 G A 26 GENIC homozygous 116766738 10 43767523 43767524 C T 37 GENIC homozygous 116766740 10 43767572 43767573 A T 37 GENIC homozygous 116766742 10 43767700 43767701 C T 11 GENIC homozygous 117128474 10 43768258 43768259 G A 27 GENIC homozygous 116766744