chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 26828799 26828800 T C 33 GENIC homozygous 114302992 13 26830750 26830751 A G 20 GENIC homozygous 114302993 13 26832190 26832191 G A 36 GENIC homozygous 114516502 13 26832404 26832405 G T 17 GENIC homozygous 114302994 13 26833370 26833371 A T 30 GENIC homozygous 114302996 13 26835827 26835828 T C 26 GENIC homozygous 114302998 13 26837977 26837978 G A 25 GENIC homozygous 114516504 13 26838237 26838238 C T 20 GENIC homozygous 114516506 13 26838286 26838287 C T 29 GENIC homozygous 114516508 13 26838402 26838403 G A 28 GENIC homozygous 114516510 13 26838417 26838418 G C 31 GENIC homozygous 114516512 13 26838778 26838779 A G 22 GENIC homozygous 114516514 13 26838998 26838999 A G 28 GENIC homozygous 114303002 13 26839148 26839149 G A 32 GENIC homozygous 114516516 13 26839715 26839716 T C 39 GENIC homozygous 114516518 13 26839750 26839751 T C 43 GENIC homozygous 114516520 13 26839801 26839802 G C 46 GENIC homozygous 114516522 13 26840498 26840499 G A 28 GENIC possibly homozygous 114516524 13 26841955 26841956 G A 21 GENIC homozygous 114516526 13 26844460 26844461 A G 28 GENIC homozygous 114516528 13 26845383 26845384 C A 13 GENIC homozygous 114303020 13 26845790 26845791 A G 12 GENIC homozygous 114303021 13 26846131 26846132 C A 25 GENIC homozygous 114303023