chr start stop reference nuc variant nuc depth genic status zygosity variant ID 1 178527033 178527034 A G 36 GENIC homozygous 992686513 1 178527146 178527147 A G 25 GENIC homozygous 992686514 1 178527407 178527408 C T 35 GENIC possibly homozygous 992686515 1 178527491 178527492 C T 27 GENIC possibly homozygous 992686516 1 178527527 178527528 C T 27 GENIC homozygous 992686517 1 178527838 178527839 A C 19 GENIC homozygous 992686518 1 178527840 178527841 T C 19 GENIC homozygous 992686519 1 178527932 178527933 T C 23 GENIC possibly homozygous 992686520 1 178528043 178528044 T A 25 GENIC homozygous 992686521 1 178528053 178528054 T C 24 GENIC homozygous 992686522 1 178528362 178528363 A G 34 GENIC possibly homozygous 992686523 1 178528372 178528373 G A 33 GENIC possibly homozygous 992686524 1 178528382 178528383 A G 32 GENIC possibly homozygous 992686525 1 178528591 178528592 C T 23 GENIC homozygous 992686526 1 178528663 178528664 C G 23 GENIC homozygous 992686527 1 178528698 178528699 T A 22 GENIC homozygous 992686528 1 178528746 178528747 T C 19 GENIC homozygous 992686529 1 178528787 178528788 T C 17 GENIC homozygous 992686530 1 178528963 178528964 A G 23 GENIC homozygous 992686531 1 178528991 178528992 T C 21 GENIC homozygous 992686532 1 178528993 178528994 G C 21 GENIC homozygous 992686533 1 178529004 178529005 G A 20 GENIC possibly homozygous 992686534 1 178529018 178529019 T C 26 GENIC possibly homozygous 992686535 1 178530290 178530291 A G 16 GENIC possibly homozygous 992686536 1 178530738 178530739 C A 27 GENIC homozygous 992686537 1 178531549 178531550 T C 19 GENIC homozygous 992686538 1 178531581 178531582 C T 22 GENIC homozygous 992686539 1 178531623 178531624 T G 26 GENIC homozygous 992686540 1 178531930 178531931 T C 26 GENIC homozygous 992686541 1 178533353 178533354 T C 34 GENIC possibly homozygous 992686542 1 178533797 178533798 A G 18 GENIC homozygous 992686543 1 178534097 178534098 A G 17 GENIC homozygous 992686544 1 178534954 178534955 C G 18 GENIC possibly homozygous 992686545