chr start stop reference nuc variant nuc depth genic status zygosity variant ID 14 104475184 104475185 T A 23 GENIC homozygous 113530450 14 104485550 104485551 C T 25 GENIC homozygous 113530452 14 104485640 104485641 C T 8 GENIC homozygous 113927805 14 104485938 104485939 A C 14 GENIC homozygous 114166543 14 104487534 104487535 G A 30 GENIC homozygous 113530454 14 104493931 104493932 T C 31 GENIC homozygous 113530456 14 104495227 104495228 C T 6 GENIC homozygous 114093228 14 104495232 104495233 G A 4 GENIC homozygous 118724104 14 104495233 104495234 G C 4 GENIC homozygous 118724105 14 104495481 104495482 G A 15 GENIC homozygous 113530458 14 104496470 104496471 A T 17 GENIC homozygous 113530460 14 104496514 104496515 G A 24 GENIC homozygous 113530462 14 104496834 104496835 G A 25 GENIC homozygous 113530464 14 104497876 104497877 A G 24 GENIC homozygous 113530466 14 104499300 104499301 A T 29 GENIC homozygous 113530468 14 104499674 104499675 C T 39 GENIC heterozygous 118724107 14 104499714 104499715 A T 53 GENIC heterozygous 118724108 14 104489880 104489881 G T 11 GENIC heterozygous 118797622 14 104499489 104499490 A T 27 GENIC heterozygous 118797623 14 104499535 104499536 C A 30 GENIC heterozygous 118797624 14 104499545 104499546 G T 26 GENIC heterozygous 118797625 14 104491325 104491326 A C 18 GENIC possibly homozygous 113827390