chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
15	36896185	36896186	G	GT	34	GENIC	homozygous	48282401
15	36896365	36896366	G	-	47	GENIC	homozygous	48282402
15	36897905	36897906	G	T	37	GENIC	homozygous	48499278
15	36898901	36898902	A	-	22	GENIC	homozygous	48499280
15	36900488	36900489	A	G	18	GENIC	possibly homozygous	48499282
15	36900587	36900588	G	GT	18	GENIC	homozygous	48499284
15	36901336	36901337	C	T	35	GENIC	homozygous	48499286
15	36902823	36902824	C	T	27	GENIC	homozygous	48499288
15	36902854	36902855	C	T	25	GENIC	homozygous	48499290
15	36902886	36902887	A	G	24	GENIC	homozygous	48499292
15	36903383	36903384	G	A	39	GENIC	homozygous	48499294
15	36928781	36928787	ATATAT	------	30	GENIC	heterozygous	48282405
15	36928808	36928809	T	C	27	GENIC	heterozygous	48584983
15	36928821	36928822	A	AGG	19	GENIC	heterozygous	48499968
15	36928828	36928829	T	G	18	GENIC	heterozygous	48282406
15	36928831	36928833	AT	--	11	GENIC	heterozygous	48282407
15	36928836	36928837	T	C	11	GENIC	heterozygous	48584987
15	36932131	36932136	TGCAT	-----	19	GENIC	heterozygous	48282410
15	36936632	36936633	C	CTT	14	GENIC	homozygous	48282411
15	36939757	36939758	A	G	15	GENIC	heterozygous	48282412
15	36931927	36931928	C	-	14	GENIC	heterozygous	48700695