chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	100131579	100131580	A	G	24	GENIC	homozygous	108898305
1	100131616	100131617	C	G	19	GENIC	homozygous	108898306
1	100131640	100131641	C	G	23	GENIC	homozygous	108898307
1	100131729	100131730	A	C	43	GENIC	possibly homozygous	108898308
1	100131833	100131834	T	C	32	GENIC	homozygous	108898309
1	100131874	100131875	C	T	28	GENIC	homozygous	108898310
1	100131901	100131902	C	T	29	GENIC	homozygous	108898311
1	100131973	100131974	A	C	37	GENIC	possibly homozygous	108898312
1	100132507	100132508	A	G	61	GENIC	homozygous	108898313
1	100132612	100132613	A	G	41	GENIC	homozygous	108898314
1	100132930	100132931	T	C	35	GENIC	homozygous	108898315
1	100133078	100133079	T	C	33	GENIC	possibly homozygous	108898316
1	100133110	100133111	T	G	31	GENIC	possibly homozygous	108898317
1	100133359	100133360	G	C	7	GENIC	heterozygous	129853243
1	100133385	100133386	T	C	12	GENIC	homozygous	108898319
1	100133545	100133546	A	G	46	GENIC	homozygous	108898320
1	100133653	100133654	G	A	46	GENIC	homozygous	108898321
1	100133913	100133914	G	A	44	GENIC	homozygous	108898322
1	100133971	100133972	A	G	45	GENIC	homozygous	108898323
1	100134039	100134040	A	G	45	GENIC	homozygous	108898324
1	100134163	100134164	G	A	49	GENIC	homozygous	108898325
1	100134397	100134398	G	A	38	GENIC	homozygous	108898326
1	100134454	100134455	T	C	46	GENIC	homozygous	108898327
1	100134593	100134594	T	C	44	GENIC	homozygous	108898328
1	100134775	100134776	C	T	34	GENIC	homozygous	108898329
1	100134859	100134861	CC		37	GENIC	homozygous	130818308
1	100134350	100134352	TG		33	GENIC	homozygous	130818306
1	100134386	100134386		CCTTTCTGTGTG	37	GENIC	homozygous	130818307
1	100135335	100135336	T	C	42	GENIC	homozygous	108898330