chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	170597358	170597359	G	A	22	GENIC	homozygous	108376209
1	170597788	170597789	G	A	31	GENIC	homozygous	108376211
1	170598294	170598295	T	C	35	GENIC	homozygous	108376213
1	170600154	170600155	C	T	19	GENIC	homozygous	108376215
1	170600834	170600835	C	A	28	GENIC	homozygous	108376217
1	170601709	170601710	A	T	19	GENIC	homozygous	108376219
1	170606236	170606237	A	G	20	GENIC	homozygous	108376223
1	170606965	170606966	C	T	18	GENIC	homozygous	108376227
1	170607688	170607689	C	T	33	GENIC	homozygous	108376229
1	170609062	170609063	C	T	26	GENIC	homozygous	108376231
1	170609109	170609110	T	C	21	GENIC	homozygous	108376234
1	170609945	170609946	T	C	18	GENIC	homozygous	108376236
1	170610794	170610795	A	G	16	GENIC	homozygous	108376238
1	170610870	170610871	C	A	12	GENIC	homozygous	108376240
1	170611061	170611062	C	T	31	GENIC	homozygous	108376242
1	170611828	170611829	C	T	22	GENIC	homozygous	108376244
1	170614080	170614081	A	G	24	GENIC	homozygous	108376246
1	170615839	170615840	C	T	23	GENIC	possibly homozygous	108376248
1	170616208	170616209	C	T	21	GENIC	homozygous	108376250
1	170616360	170616361	C	T	21	GENIC	homozygous	108376252
1	170619031	170619032	C	T	19	GENIC	homozygous	108376254
1	170619252	170619253	C	T	19	GENIC	homozygous	108376256
1	170620820	170620821	T	G	23	GENIC	homozygous	108376258
1	170621609	170621610	G	A	27	GENIC	homozygous	108376260
1	170622757	170622758	T	C	16	GENIC	homozygous	108376262
1	170615184	170615185	C		25	GENIC	possibly homozygous	127455559
1	170615343	170615344	G		20	GENIC	homozygous	127455560
1	170625577	170625578	C	T	20	GENIC	homozygous	108376264
1	170626457	170626458	G	A	25	GENIC	homozygous	108376266
1	170628568	170628569	G	A	17	GENIC	homozygous	108376268
1	170628428	170628429	T	A	21	GENIC	homozygous	108958866