chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	100181681	100181682	A	G	49	GENIC	homozygous	112798284
4	100183655	100183656	C	T	22	GENIC	homozygous	112798287
4	100185098	100185099	C	T	32	GENIC	homozygous	113537197
4	100185538	100185539	C	T	29	GENIC	homozygous	113537199
4	100186813	100186814	C	A	18	GENIC	homozygous	112798291
4	100187211	100187212	C	T	25	GENIC	homozygous	113537201
4	100188487	100188488	A	G	26	GENIC	possibly homozygous	113537203
4	100189019	100189020	A	G	27	GENIC	homozygous	113537205
4	100189103	100189104	G	A	19	GENIC	homozygous	113537207
4	100189332	100189333	T	C	25	GENIC	homozygous	113537209
4	100189514	100189515	C	G	26	GENIC	homozygous	113537211
4	100189711	100189712	G	A	25	GENIC	heterozygous	112798297
4	100189738	100189739	A	G	26	GENIC	heterozygous	113537213
4	100189937	100189938	A	G	42	GENIC	heterozygous	112798303
4	100191591	100191592	G	A	19	GENIC	homozygous	112798313
4	100192567	100192568	G	C	36	GENIC	homozygous	112798315
4	100193950	100193951	C	G	37	GENIC	homozygous	113537215
4	100195344	100195345	T	C	26	GENIC	homozygous	112798320
4	100199550	100199551	G	T	37	GENIC	homozygous	113537217
4	100199941	100199942	G	A	22	GENIC	homozygous	112798324
4	100199969	100199970	C	T	27	GENIC	homozygous	112798326
4	100200661	100200662	C	T	21	GENIC	homozygous	113537219
4	100201445	100201446	C	A	38	GENIC	homozygous	113537221
4	100206538	100206539	T	G	18	GENIC	homozygous	112798353
4	100209553	100209554	C	T	27	GENIC	homozygous	112798362