chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	104417056	104417057	G	A	29	GENIC	homozygous	109959245
2	104417617	104417618	C	A	18	GENIC	homozygous	109959247
2	104418511	104418512	A	T	20	GENIC	homozygous	109959249
2	104419736	104419737	T	C	27	GENIC	homozygous	109959251
2	104421788	104421789	T	A	30	GENIC	homozygous	109959253
2	104426561	104426562	T	C	32	GENIC	homozygous	109959255
2	104428131	104428132	A	T	30	GENIC	homozygous	109959257
2	104430493	104430494	C	T	28	GENIC	homozygous	109959261
2	104430649	104430650	T	C	33	GENIC	homozygous	109959263
2	104430725	104430726	C	T	41	GENIC	homozygous	109959265
2	104430786	104430787	G	A	32	GENIC	homozygous	109959267
2	104431742	104431743	T	C	23	GENIC	homozygous	109959269
2	104431819	104431820	G	T	9	GENIC	homozygous	109959271
2	104434996	104434997	G	A	31	GENIC	homozygous	109959279
2	104437039	104437040	T	A	38	GENIC	homozygous	109959283
2	104440119	104440120	C	G	34	GENIC	homozygous	109959287
2	104442506	104442507	A	G	26	GENIC	homozygous	109959289
2	104444459	104444460	C	T	32	GENIC	homozygous	109959291
2	104444504	104444505	T	C	35	GENIC	homozygous	109959293
2	104446850	104446851	A	G	24	GENIC	homozygous	109959294
2	104447406	104447407	G	T	27	GENIC	homozygous	109959296
2	104448149	104448150	A	T	10	GENIC	homozygous	109959298
2	104448968	104448969	G	A	34	GENIC	homozygous	109959306
2	104450398	104450399	G	A	35	GENIC	homozygous	109959308
2	104452193	104452194	A	G	21	GENIC	homozygous	109959310
2	104453026	104453027	G	C	26	GENIC	homozygous	109959316
2	104453569	104453570	T	C	14	GENIC	homozygous	111257120
2	104455762	104455763	C	T	25	GENIC	homozygous	111257124
2	104456330	104456331	G	A	8	GENIC	homozygous	111257126
2	104458119	104458120	C	T	16	GENIC	homozygous	120369262
2	104450475	104450476	C	T	20	GENIC	homozygous	120369259
2	104450599	104450600	G	A	20	GENIC	homozygous	120369260
2	104455341	104455342	C	T	29	GENIC	homozygous	120369261
2	104458997	104458998	T	C	15	GENIC	homozygous	109959353