chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	10277802	10277803	A	G	20	GENIC	homozygous	111722582
16	10278626	10278627	A	G	20	GENIC	homozygous	111722584
16	10279376	10279377	T	G	8	GENIC	homozygous	111722586
16	10279967	10279968	G	A	9	GENIC	homozygous	111722588
16	10280217	10280218	G	A	7	GENIC	homozygous	111722590
16	10281399	10281400	T	A	27	GENIC	homozygous	111933052
16	10279400	10279401	T	C	13	GENIC	homozygous	111933046
16	10279661	10279662	A	G	15	GENIC	homozygous	111933048
16	10280684	10280685	G	A	19	GENIC	homozygous	111933050
16	10281793	10281794	C	T	27	GENIC	homozygous	111933054
16	10281887	10281888	G	C	19	GENIC	homozygous	111933056
16	10282011	10282012	G	T	32	GENIC	homozygous	111722603
16	10282172	10282173	A	G	20	GENIC	homozygous	111722605
16	10283022	10283023	A	T	16	GENIC	homozygous	111933058
16	10283027	10283028	A	C	16	GENIC	homozygous	111933060
16	10283402	10283403	C	T	12	GENIC	homozygous	111722619
16	10283460	10283461	C	A	19	GENIC	homozygous	111722621
16	10283685	10283686	A	G	15	GENIC	homozygous	111722623
16	10283695	10283696	A	G	21	GENIC	homozygous	111933062
16	10283768	10283769	C	T	19	GENIC	homozygous	111933064
16	10283885	10283886	A	G	23	GENIC	homozygous	111722625
16	10283896	10283897	C	T	22	GENIC	homozygous	111722627
16	10281468	10281469	C	T	23	GENIC	homozygous	112050603
16	10284090	10284091	C	T	19	GENIC	homozygous	111722633
16	10284528	10284529	C	T	26	GENIC	homozygous	111933068
16	10284910	10284911	C	T	30	GENIC	homozygous	111722637
16	10285191	10285192	C	T	25	GENIC	homozygous	111933070
16	10285348	10285349	A	G	25	GENIC	homozygous	111722639
16	10285542	10285543	C	T	33	GENIC	homozygous	111722641