chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	80367214	80367215	G	T	16	GENIC	homozygous	111635291
3	80367251	80367252	T	G	17	GENIC	homozygous	119650324
3	80367254	80367255	T	G	18	GENIC	homozygous	119650325
3	80367259	80367260	G	T	22	GENIC	homozygous	119650326
3	80371633	80371634	C	T	16	GENIC	homozygous	111635292
3	80371908	80371909	C	G	20	GENIC	homozygous	111635293
3	80379050	80379051	G	T	35	GENIC	homozygous	111635294
3	80382022	80382023	T	A	14	GENIC	homozygous	111635297
3	80386805	80386806	G	T	19	GENIC	homozygous	111635301
3	80387088	80387089	G	A	17	GENIC	homozygous	111635302
3	80389828	80389829	T	C	35	GENIC	homozygous	111635305
3	80390732	80390733	G	A	28	GENIC	homozygous	112390334
3	80394787	80394788	C	T	24	GENIC	homozygous	111635309
3	80399052	80399053	C	T	19	GENIC	homozygous	112390335
3	80399574	80399575	T	C	34	GENIC	homozygous	111635312
3	80401313	80401314	G	A	26	GENIC	homozygous	112241979
3	80401823	80401824	A	C	30	GENIC	homozygous	112241981
3	80403380	80403381	T	A	26	GENIC	homozygous	111635315
3	80403581	80403582	A	G	20	GENIC	homozygous	111950267
3	80406423	80406424	T	C	14	GENIC	homozygous	111635319
3	80403813	80403814	C	T	17	GENIC	homozygous	112390336
3	80403928	80403929	C	T	11	GENIC	homozygous	111635316
3	80404384	80404385	T	A	35	GENIC	homozygous	112241982
3	80411784	80411785	A	G	19	GENIC	homozygous	111635335