chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	91128208	91128209	T	A	16	GENIC	homozygous	117088139
10	91129448	91129449	A	G	18	GENIC	homozygous	117020662
10	91130235	91130236	G	T	24	GENIC	homozygous	117088141
10	91131882	91131883	G	A	30	GENIC	homozygous	117088143
10	91132345	91132346	T	C	9	GENIC	homozygous	117088145
10	91134392	91134393	A	G	32	GENIC	homozygous	116905425
10	91135716	91135717	A	G	28	GENIC	homozygous	116905431
10	91139931	91139932	G	A	24	GENIC	homozygous	117088151
10	91140303	91140304	A	T	13	GENIC	homozygous	116905435
10	91140304	91140305	G	A	13	GENIC	homozygous	116905437
10	91141239	91141240	T	C	22	GENIC	homozygous	116905439
10	91142117	91142118	G	T	20	GENIC	homozygous	117088153
10	91142401	91142402	C	T	25	GENIC	homozygous	117088155
10	91146554	91146555	T	C	43	GENIC	homozygous	116905441
10	91146730	91146731	C	T	38	GENIC	homozygous	117088161
10	91147362	91147363	A	G	18	GENIC	homozygous	116905443
10	91148068	91148069	C	T	41	GENIC	homozygous	117088163
10	91149470	91149471	A	G	40	GENIC	homozygous	116905445
10	91149559	91149560	A	T	36	GENIC	homozygous	116905447
10	91149579	91149580	T	C	39	GENIC	homozygous	116905449
10	91150735	91150736	T	C	43	GENIC	homozygous	116905451
10	91153707	91153708	C	T	23	GENIC	homozygous	117088165
10	91154119	91154120	T	C	39	GENIC	homozygous	117088167
10	91154133	91154134	T	C	38	GENIC	homozygous	117088169
10	91158633	91158634	T	C	32	GENIC	homozygous	117088171
10	91159484	91159485	G	A	40	GENIC	homozygous	117105270
10	91160010	91160011	C	T	35	GENIC	homozygous	116951768
10	91160311	91160312	A	G	36	GENIC	homozygous	116905461