chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	150689860	150689861	A	-	3	GENIC	homozygous	55794303
5	150691202	150691203	A	G	21	GENIC	homozygous	55794307
5	150691959	150691960	T	C	19	GENIC	possibly homozygous	55794308
5	150692638	150692639	T	C	21	GENIC	possibly homozygous	55794311
5	150693001	150693002	A	G	2	GENIC	homozygous	55794312
5	150693275	150693276	A	G	10	GENIC	possibly homozygous	55794313
5	150693616	150693617	T	C	14	GENIC	homozygous	55794314
5	150693673	150693674	A	G	21	GENIC	homozygous	55794315
5	150693730	150693731	T	C	27	GENIC	possibly homozygous	55794316
5	150695158	150695159	A	G	24	GENIC	possibly homozygous	55794318
5	150695273	150695274	T	C	22	GENIC	homozygous	55794319
5	150695708	150695709	C	T	31	GENIC	possibly homozygous	55794321
5	150696202	150696203	T	C	24	GENIC	possibly homozygous	55794322
5	150696582	150696583	G	C	10	GENIC	heterozygous	55794323
5	150696929	150696930	A	ATG	1	GENIC	homozygous	55794332
5	150698648	150698649	C	T	9	GENIC	possibly homozygous	55794334
5	150700645	150700646	G	A	12	GENIC	heterozygous	55794335
5	150702261	150702262	G	T	11	GENIC	possibly homozygous	55794336
5	150703488	150703489	G	T	15	GENIC	homozygous	55794338
5	150696694	150696695	C	CTGTGTGTCTGTGTG	1	GENIC	homozygous	56460609
5	150703291	150703292	G	T	11	GENIC	homozygous	55794337
5	150705160	150705161	T	TA	4	GENIC	heterozygous	55794339
5	150705460	150705462	AA	--	1	GENIC	homozygous	55924122
5	150712090	150712091	C	CCAGGCTCTGCCG	3	GENIC	homozygous	55794342
5	150713327	150713328	G	GTGAATGAT	6	GENIC	homozygous	55794343
5	150720787	150720788	C	T	3	GENIC	homozygous	55794347
5	150722133	150722134	A	-	4	GENIC	heterozygous	55794348