chr start stop reference nuc variant nuc depth genic status zygosity variant ID 18 11941942 11941943 C T 14 GENIC homozygous 140263015 18 11942131 11942132 G A 31 GENIC homozygous 140263016 18 11942643 11942644 G A 23 GENIC homozygous 140263017 18 11942651 11942652 T C 24 GENIC homozygous 140263018 18 11943261 11943262 A G 14 GENIC homozygous 140263019 18 11943390 11943390 A 18 GENIC homozygous 140209846 18 11943401 11943402 A T 17 GENIC homozygous 140263020 18 11943803 11943804 G A 14 GENIC homozygous 140263021 18 11945763 11945764 A G 26 GENIC homozygous 140263022 18 11946651 11946652 A C 11 GENIC homozygous 140263023 18 11947930 11947931 C T 19 GENIC homozygous 140263024 18 11948278 11948279 A G 19 GENIC homozygous 140263025 18 11948569 11948570 A C 26 GENIC homozygous 140263026 18 11948778 11948779 G A 18 GENIC homozygous 140263027 18 11949332 11949335 TTC 22 GENIC homozygous 140209850 18 11944369 11944369 AAA 8 GENIC homozygous 140209847 18 11948384 11948384 C 7 GENIC homozygous 140209848 18 11948948 11948950 AT 15 GENIC homozygous 140209849 18 11949393 11949394 A G 23 GENIC homozygous 140263028 18 11949450 11949451 A G 23 GENIC homozygous 140263029 18 11949747 11949748 T 21 GENIC possibly homozygous 140209851 18 11950509 11950510 G A 25 GENIC homozygous 140263030