chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	80367214	80367215	G	T	18	GENIC	homozygous	111635291
3	80367251	80367252	T	G	13	GENIC	homozygous	119650324
3	80367254	80367255	T	G	14	GENIC	homozygous	119650325
3	80367259	80367260	G	T	15	GENIC	homozygous	119650326
3	80371633	80371634	C	T	24	GENIC	homozygous	111635292
3	80371908	80371909	C	G	22	GENIC	homozygous	111635293
3	80382022	80382023	T	A	21	GENIC	homozygous	111635297
3	80386805	80386806	G	T	19	GENIC	homozygous	111635301
3	80387088	80387089	G	A	21	GENIC	homozygous	111635302
3	80387859	80387860	C	T	26	GENIC	homozygous	111635303
3	80389828	80389829	T	C	27	GENIC	homozygous	111635305
3	80392627	80392628	T	C	15	GENIC	homozygous	111635306
3	80393098	80393099	G	A	14	GENIC	homozygous	111635307
3	80394309	80394310	T	C	21	GENIC	homozygous	111635308
3	80394787	80394788	C	T	23	GENIC	homozygous	111635309
3	80396068	80396069	C	T	24	GENIC	homozygous	111635310
3	80396242	80396243	C	T	22	GENIC	possibly homozygous	111635311
3	80399574	80399575	T	C	29	GENIC	homozygous	111635312
3	80402942	80402943	T	C	26	GENIC	homozygous	111635314
3	80403380	80403381	T	A	22	GENIC	homozygous	111635315
3	80403928	80403929	C	T	10	GENIC	homozygous	111635316
3	80405160	80405161	G	A	18	GENIC	possibly homozygous	111635317
3	80406423	80406424	T	C	17	GENIC	homozygous	111635319
3	80407440	80407441	T	C	23	GENIC	homozygous	111635320
3	80410332	80410333	G	A	24	GENIC	homozygous	111635326
3	80411412	80411413	G	A	8	GENIC	homozygous	111635334
3	80412011	80412012	T	G	23	GENIC	homozygous	111635336
3	80414072	80414073	A	G	20	GENIC	homozygous	111635337
3	80414664	80414665	T	C	26	GENIC	homozygous	111635338
3	80415733	80415734	C	T	31	GENIC	homozygous	111635339
3	80416234	80416235	C	G	22	GENIC	homozygous	111635340