chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	107843900	107843901	G	A	22	GENIC	homozygous	49188225
14	107843902	107843903	T	C	21	GENIC	homozygous	48891656
14	107844771	107844772	A	G	26	GENIC	homozygous	49188227
14	107845206	107845207	G	A	30	GENIC	homozygous	49188229
14	107846540	107846541	C	T	31	GENIC	homozygous	49188231
14	107848917	107848918	G	A	23	GENIC	possibly homozygous	49188233
14	107849445	107849446	C	T	16	GENIC	homozygous	49188235
14	107849454	107849455	T	C	20	GENIC	homozygous	49188237
14	107849648	107849649	A	AAAAG	22	GENIC	homozygous	49188239
14	107851120	107851121	G	A	28	GENIC	homozygous	49188241
14	107851937	107851938	C	CA	16	GENIC	homozygous	49188243
14	107853466	107853476	GTGTGTGTGT	----------	3	GENIC	homozygous	49352277
14	107849885	107849886	C	CTTT	5	GENIC	heterozygous	49422188
14	107851703	107851704	T	TTGGAATGTGTGTAAACTACGTGTGTG	31	GENIC	homozygous	49321068
14	107851707	107851708	G	T	31	GENIC	homozygous	49321069
14	107851716	107851717	G	GTCATTCC	26	GENIC	homozygous	49321070
14	107854130	107854131	G	A	26	GENIC	homozygous	49188245
14	107854323	107854324	G	A	30	GENIC	homozygous	49188247
14	107854413	107854434	GCATGCACCAGGTGTGGTGGG	---------------------	19	GENIC	homozygous	49188249
14	107854154	107854155	C	CTGTGTGTGTGTGTGTGTA	14	GENIC	homozygous	49293280