chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	150672504	150672505	G	C	21	GENIC	homozygous	55794269
5	150673672	150673673	G	GTTGTT	1	GENIC	homozygous	55794270
5	150674660	150674661	A	G	21	GENIC	homozygous	55794272
5	150675487	150675488	C	-	21	GENIC	homozygous	55794274
5	150675637	150675638	T	C	13	GENIC	possibly homozygous	55794275
5	150676315	150676316	A	AT	13	GENIC	possibly homozygous	55794277
5	150676716	150676717	T	C	23	GENIC	homozygous	55794278
5	150676901	150676902	G	A	21	GENIC	possibly homozygous	55794279
5	150677109	150677110	C	CTA	11	GENIC	heterozygous	55794280
5	150677302	150677303	T	C	28	GENIC	possibly homozygous	55794281
5	150677603	150677604	C	T	16	GENIC	homozygous	55794282
5	150678131	150678132	C	T	17	GENIC	possibly homozygous	55794283
5	150678247	150678248	A	C	22	GENIC	possibly homozygous	55794284
5	150678296	150678297	A	G	11	GENIC	homozygous	55794285
5	150678319	150678320	T	C	9	GENIC	homozygous	55794286
5	150678978	150678979	C	T	16	GENIC	possibly homozygous	55794287
5	150679780	150679781	A	G	9	GENIC	homozygous	55794290
5	150680266	150680267	G	A	30	GENIC	homozygous	55794292
5	150680435	150680436	T	G	10	GENIC	possibly homozygous	55794293
5	150680756	150680757	C	T	15	GENIC	possibly homozygous	55794294
5	150681747	150681748	T	C	5	GENIC	homozygous	55794297
5	150683300	150683301	C	T	13	GENIC	possibly homozygous	55794298