chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	209099596	209099597	A	C	11	GENIC	homozygous	110220350
2	209099662	209099663	T	A	12	GENIC	homozygous	110220351
2	209099680	209099681	T	C	7	GENIC	homozygous	110220352
2	209099861	209099862	C	T	19	GENIC	homozygous	110814141
2	209099935	209099936	G	A	10	GENIC	homozygous	110220353
2	209100005	209100006	C	T	9	GENIC	homozygous	110220354
2	209100315	209100316	C	T	12	GENIC	homozygous	110220355
2	209101863	209101864	G	T	18	GENIC	homozygous	110220356
2	209102263	209102264	T	C	16	GENIC	homozygous	110220357
2	209103443	209103444	G	A	22	GENIC	homozygous	110220361
2	209103587	209103588	A	G	17	GENIC	homozygous	110220362
2	209103758	209103759	A	G	21	GENIC	homozygous	110220363
2	209104618	209104619	A	T	12	GENIC	homozygous	110220365
2	209104890	209104891	C	T	10	GENIC	homozygous	110220366
2	209104902	209104903	G	A	7	GENIC	homozygous	110814145
2	209105067	209105068	G	A	10	GENIC	homozygous	110220368
2	209105496	209105497	A	G	10	GENIC	homozygous	110220369
2	209107100	209107101	A	G	23	GENIC	homozygous	110220370
2	209107147	209107148	G	T	26	GENIC	homozygous	110220371
2	209109264	209109265	T	G	20	GENIC	homozygous	110220373
2	209109518	209109519	G	A	17	GENIC	homozygous	110814147
2	209109814	209109815	A	T	19	GENIC	homozygous	110220374
2	209112363	209112364	C	T	11	GENIC	homozygous	110814149
2	209112376	209112377	A	G	13	GENIC	homozygous	110814151
2	209112857	209112858	A	G	30	GENIC	possibly homozygous	110814153
2	209113337	209113338	A	G	20	GENIC	homozygous	110220378
2	209113399	209113400	T	A	20	GENIC	homozygous	110220379
2	209113928	209113929	T	C	21	GENIC	homozygous	110814155
2	209114066	209114067	A	G	14	GENIC	homozygous	110814157
2	209114563	209114564	T	G	6	GENIC	homozygous	110814159
2	209114735	209114736	A	C	17	GENIC	homozygous	110814161
2	209114824	209114825	A	T	11	GENIC	homozygous	110814163
2	209116304	209116305	G	A	15	GENIC	homozygous	110814165