chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	29986318	29986318		A	21	GENIC	homozygous	140018383
17	29991576	29991577	C	T	18	GENIC	homozygous	140094997
17	29992373	29992374	T	C	30	GENIC	homozygous	140094998
17	29992887	29992888	T	C	26	GENIC	homozygous	140094999
17	29993074	29993075	C	G	15	GENIC	homozygous	140095000
17	29995924	29995925	T		22	GENIC	possibly homozygous	140018384
17	29996154	29996154		A	16	GENIC	possibly homozygous	140018385
17	29996634	29996635	C	G	16	GENIC	homozygous	140095001
17	29997772	29997773	T	G	20	GENIC	homozygous	140095002
17	29999359	29999361	AG		19	GENIC	homozygous	140018386
17	29999743	29999744	T	C	12	GENIC	homozygous	140095003
17	30000052	30000053	A	G	24	GENIC	homozygous	140095004
17	30000071	30000072	C	T	24	GENIC	homozygous	140095005
17	30001903	30001904	A	G	19	GENIC	homozygous	140095006
17	30003819	30003820	T	G	13	GENIC	homozygous	140095007
17	30005478	30005482	AAAT		20	GENIC	homozygous	140018388
17	30005689	30005690	A	G	25	GENIC	homozygous	140095008
17	30006666	30006667	T	A	27	GENIC	homozygous	140095009
17	30007070	30007071	G	T	16	GENIC	homozygous	140095010
17	30008503	30008504	G	A	16	GENIC	homozygous	140095014
17	30007735	30007736	T	C	26	GENIC	homozygous	140095011
17	30007917	30007918	A	G	17	GENIC	homozygous	140095012
17	30008032	30008033	G	A	18	GENIC	homozygous	140095013
17	30010208	30010209	A		14	GENIC	homozygous	140018389
17	30011996	30011997	T	C	16	GENIC	homozygous	140095015
17	30013917	30013918	G	T	23	GENIC	possibly homozygous	140095016
17	30014707	30014708	T		14	GENIC	homozygous	140018390
17	30014760	30014761	C	T	9	GENIC	homozygous	140095017
17	30015057	30015058	A	G	17	GENIC	homozygous	140095018
17	30016522	30016523	C	T	15	GENIC	homozygous	140095019
17	30016791	30016792	T	G	9	GENIC	homozygous	140095020
17	30017359	30017360	C	T	21	GENIC	homozygous	140095021
17	30017442	30017443	A		21	GENIC	homozygous	140018391