chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	92269075	92269076	G	T	4	GENIC	homozygous	56039329
5	92269612	92269613	C	CG	9	GENIC	homozygous	56039330
5	92269749	92269750	A	G	12	GENIC	possibly homozygous	56170163
5	92269820	92269821	C	T	23	GENIC	homozygous	56039331
5	92270563	92270564	G	T	10	GENIC	homozygous	56039333
5	92270583	92270588	TTCTG	-----	7	GENIC	homozygous	56039334
5	92270723	92270724	T	C	18	GENIC	homozygous	56039335
5	92271050	92271051	A	G	3	GENIC	homozygous	56039336
5	92271089	92271090	G	A	8	GENIC	homozygous	56039337
5	92271322	92271323	T	TA	12	GENIC	homozygous	56039338
5	92272505	92272506	C	T	22	GENIC	homozygous	56039339
5	92272790	92272791	G	T	23	GENIC	possibly homozygous	56039340
5	92272838	92272839	G	T	20	GENIC	homozygous	56039341
5	92272913	92272914	A	G	20	GENIC	homozygous	56039342
5	92273832	92273833	T	C	13	GENIC	homozygous	56039343
5	92274188	92274189	C	T	13	GENIC	homozygous	55559943
5	92274598	92274599	G	A	24	GENIC	homozygous	56039344
5	92274645	92274646	A	C	24	GENIC	homozygous	56039345
5	92274922	92274923	A	G	15	GENIC	homozygous	56039346
5	92275069	92275070	G	A	21	GENIC	homozygous	56039347
5	92275227	92275228	C	T	23	GENIC	homozygous	56170165
5	92275714	92275715	T	G	13	GENIC	homozygous	56039348
5	92276027	92276028	G	A	8	GENIC	homozygous	56039349
5	92276604	92276605	C	G	18	GENIC	homozygous	56039350