chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	36487948	36487949	G	T	19	GENIC	homozygous	51414343
10	36488259	36488260	T	C	20	GENIC	possibly homozygous	51414345
10	36488775	36488776	C	A	13	GENIC	heterozygous	51414347
10	36489623	36489624	A	G	19	GENIC	homozygous	51414349
10	36490728	36490729	A	G	11	GENIC	homozygous	51414351
10	36491441	36491442	A	-	1	GENIC	homozygous	51414353
10	36491519	36491520	G	A	15	GENIC	possibly homozygous	51414355
10	36492877	36492878	A	G	19	GENIC	possibly homozygous	51414359
10	36493505	36493506	A	G	18	GENIC	possibly homozygous	51414361
10	36493559	36493560	A	G	12	GENIC	homozygous	51414363
10	36494731	36494732	T	C	29	GENIC	homozygous	51414365
10	36494880	36494881	T	C	10	GENIC	homozygous	51414367
10	36495245	36495246	T	-	6	GENIC	homozygous	51414371
10	36496780	36496781	A	G	33	GENIC	homozygous	51414373
10	36499279	36499280	T	-	2	GENIC	homozygous	51414375
10	36499410	36499411	G	C	14	GENIC	homozygous	51414377
10	36500031	36500032	T	TA	2	GENIC	homozygous	51414381
10	36500511	36500512	T	A	14	GENIC	possibly homozygous	51414383
10	36501696	36501697	A	T	25	GENIC	heterozygous	51414385
10	36501697	36501698	G	C	25	GENIC	heterozygous	51414387
10	36502008	36502009	T	C	18	GENIC	possibly homozygous	51414389
10	36502155	36502159	GTAG	----	9	GENIC	possibly homozygous	51414391
10	36503263	36503264	G	A	17	GENIC	homozygous	51414393
10	36504409	36504410	C	G	15	GENIC	possibly homozygous	51414395
10	36505059	36505060	C	T	10	GENIC	homozygous	51414397
10	36505067	36505068	T	G	6	GENIC	homozygous	51414399
10	36505085	36505086	T	TA	9	GENIC	homozygous	51414401