chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	11907800	11907801	T	A	15	GENIC	possibly homozygous	47366189
17	11910609	11910610	T	TAG	3	GENIC	homozygous	47366197
17	11911291	11911292	C	T	15	GENIC	homozygous	47366203
17	11911760	11911761	G	A	27	GENIC	homozygous	47366205
17	11912323	11912324	C	T	19	GENIC	homozygous	47366207
17	11913962	11913963	C	G	13	GENIC	homozygous	47021263
17	11914053	11914054	G	T	14	GENIC	homozygous	47366211
17	11914882	11914883	C	A	21	GENIC	possibly homozygous	47366213
17	11915241	11915242	C	T	19	GENIC	homozygous	47366215
17	11918398	11918399	A	T	3	GENIC	homozygous	47366221
17	11919380	11919381	T	G	23	GENIC	homozygous	47021270
17	11920580	11920581	A	T	8	GENIC	possibly homozygous	47366223
17	11921334	11921335	T	C	22	GENIC	homozygous	47021271
17	11921648	11921649	T	C	27	GENIC	possibly homozygous	47021272
17	11922389	11922390	A	G	20	GENIC	possibly homozygous	47021273
17	11923101	11923102	T	TCCCAC	1	GENIC	homozygous	47366225
17	11923113	11923114	G	C	1	GENIC	homozygous	47366227
17	11923129	11923130	T	C	5	GENIC	homozygous	47366229
17	11923183	11923184	G	C	2	GENIC	homozygous	47366231
17	11923895	11923896	A	G	8	GENIC	homozygous	47366233
17	11923991	11923992	G	A	25	GENIC	possibly homozygous	47021277