chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	104417056	104417057	G	A	44	GENIC	homozygous	109959245
2	104417617	104417618	C	A	32	GENIC	homozygous	109959247
2	104418511	104418512	A	T	30	GENIC	homozygous	109959249
2	104419736	104419737	T	C	55	GENIC	homozygous	109959251
2	104421788	104421789	T	A	11	GENIC	homozygous	109959253
2	104426561	104426562	T	C	21	GENIC	homozygous	109959255
2	104428131	104428132	A	T	28	GENIC	homozygous	109959257
2	104430118	104430119	A	G	27	GENIC	homozygous	109959259
2	104430493	104430494	C	T	27	GENIC	homozygous	109959261
2	104430649	104430650	T	C	44	GENIC	homozygous	109959263
2	104430725	104430726	C	T	45	GENIC	homozygous	109959265
2	104430786	104430787	G	A	28	GENIC	homozygous	109959267
2	104431742	104431743	T	C	35	GENIC	homozygous	109959269
2	104431819	104431820	G	T	35	GENIC	homozygous	109959271
2	104434996	104434997	G	A	33	GENIC	homozygous	109959279
2	104437039	104437040	T	A	25	GENIC	homozygous	109959283
2	104440119	104440120	C	G	32	GENIC	homozygous	109959287
2	104442506	104442507	A	G	31	GENIC	homozygous	109959289
2	104444459	104444460	C	T	43	GENIC	homozygous	109959291
2	104444504	104444505	T	C	45	GENIC	homozygous	109959293
2	104446850	104446851	A	G	13	GENIC	homozygous	109959294
2	104447406	104447407	G	T	22	GENIC	homozygous	109959296
2	104450398	104450399	G	A	26	GENIC	homozygous	109959308
2	104452193	104452194	A	G	41	GENIC	homozygous	109959310
2	104452549	104452550	C	G	23	GENIC	homozygous	109959312
2	104453026	104453027	G	C	28	GENIC	homozygous	109959316
2	104453252	104453253	G	T	37	GENIC	homozygous	109959318
2	104455762	104455763	C	T	44	GENIC	homozygous	111257124
2	104450475	104450476	C	T	26	GENIC	homozygous	120369259
2	104450599	104450600	G	A	31	GENIC	homozygous	120369260
2	104455341	104455342	C	T	48	GENIC	homozygous	120369261
2	104453569	104453570	T	C	8	GENIC	homozygous	111257120
2	104456330	104456331	G	A	32	GENIC	homozygous	111257126
2	104458119	104458120	C	T	48	GENIC	homozygous	120369262
2	104458997	104458998	T	C	22	GENIC	homozygous	109959353