chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	36487948	36487949	G	T	22	GENIC	possibly homozygous	51414343
10	36488188	36488189	C	T	5	GENIC	homozygous	52139483
10	36488212	36488213	T	C	8	GENIC	homozygous	52139485
10	36488259	36488260	T	C	5	GENIC	homozygous	51414345
10	36488775	36488776	C	A	2	GENIC	homozygous	51414347
10	36489883	36489884	G	T	21	GENIC	possibly homozygous	52139487
10	36490728	36490729	A	G	13	GENIC	homozygous	51414351
10	36491441	36491442	A	-	5	GENIC	heterozygous	51414353
10	36491519	36491520	G	A	11	GENIC	homozygous	51414355
10	36491616	36491617	A	T	19	GENIC	possibly homozygous	52139489
10	36493505	36493506	A	G	15	GENIC	possibly homozygous	51414361
10	36493559	36493560	A	G	15	GENIC	homozygous	51414363
10	36493703	36493704	G	A	10	GENIC	homozygous	52139491
10	36494731	36494732	T	C	28	GENIC	homozygous	51414365
10	36494880	36494881	T	C	16	GENIC	possibly homozygous	51414367
10	36495617	36495618	G	C	22	GENIC	possibly homozygous	52139495
10	36496095	36496096	T	C	12	GENIC	heterozygous	52139497
10	36496780	36496781	A	G	14	GENIC	homozygous	51414373
10	36499157	36499158	C	A	8	GENIC	homozygous	52139499
10	36499410	36499411	G	C	15	GENIC	possibly homozygous	51414377
10	36500511	36500512	T	A	22	GENIC	possibly homozygous	51414383
10	36502155	36502159	GTAG	----	3	GENIC	homozygous	51414391
10	36502584	36502585	T	-	16	GENIC	heterozygous	52139501
10	36502851	36502852	C	T	9	GENIC	homozygous	52139503
10	36505059	36505060	C	T	13	GENIC	homozygous	51414397
10	36505067	36505068	T	G	10	GENIC	possibly homozygous	51414399