chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	106450161	106450162	C	A	19	GENIC	homozygous	48885301
14	106453019	106453130	AAAAACTTCTGAGAGCGCTTGCCTAGGAAGCGCAAGGCCCTGGGTTCGGTCCCCAGCTCTGGAAAAAAAAAAAAAAAAAAAAAAGAACCAAAAAAAAAAAAAAAAAAAAAA	---------------------------------------------------------------------------------------------------------------	25	GENIC	homozygous	49293175
14	106453175	106453176	T	TA	27	GENIC	homozygous	48885305
14	106453531	106453532	C	T	23	GENIC	homozygous	48885307
14	106454105	106454106	C	T	13	GENIC	homozygous	48885309
14	106455139	106455140	C	T	18	GENIC	possibly homozygous	48885311
14	106455190	106455191	T	-	7	GENIC	homozygous	48885313
14	106455297	106455298	C	CCT	2	GENIC	heterozygous	48885315
14	106455448	106455449	T	C	6	GENIC	homozygous	48885321
14	106455450	106455451	G	A	6	GENIC	homozygous	48885322
14	106455504	106455506	TT	--	20	GENIC	possibly homozygous	48885324
14	106455670	106455671	T	A	20	GENIC	possibly homozygous	48885326
14	106455781	106455782	C	T	30	GENIC	possibly homozygous	48885328
14	106456112	106456113	T	C	24	GENIC	possibly homozygous	48885330
14	106456160	106456161	A	C	25	GENIC	possibly homozygous	48885332
14	106456208	106456209	C	T	29	GENIC	homozygous	48885334
14	106456544	106456545	A	AACAC	2	GENIC	homozygous	48885336
14	106457443	106457444	T	C	27	GENIC	homozygous	48885338
14	106457516	106457517	T	C	37	GENIC	possibly homozygous	48885340
14	106457915	106457916	A	AT	17	GENIC	possibly homozygous	48885342
14	106461136	106461137	G	A	34	GENIC	possibly homozygous	48885344
14	106461323	106461324	C	T	37	GENIC	possibly homozygous	48885346
14	106462222	106462224	AA	--	10	GENIC	heterozygous	48885348
14	106462223	106462224	A	-	10	GENIC	heterozygous	48885350
14	106462243	106462246	AAA	---	17	GENIC	possibly homozygous	48885354
14	106462372	106462373	T	C	25	GENIC	homozygous	48885358
14	106463105	106463106	A	G	25	GENIC	homozygous	48885360
14	106463508	106463509	C	T	24	GENIC	homozygous	48885362