chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	40701109	40701110	G	C	22	GENIC	homozygous	114767363
6	40702901	40702902	G	A	22	GENIC	homozygous	115374195
6	40703358	40703359	A	G	13	GENIC	homozygous	114767389
6	40704005	40704006	T	A	24	GENIC	homozygous	115374197
6	40705218	40705219	C	T	7	GENIC	homozygous	115374201
6	40705319	40705320	G	T	10	GENIC	homozygous	115374203
6	40705557	40705558	G	A	25	GENIC	homozygous	115374207
6	40705673	40705674	A	T	21	GENIC	homozygous	115374211
6	40705871	40705872	T	A	29	GENIC	homozygous	115205530
6	40706120	40706121	A	G	20	GENIC	homozygous	115374213
6	40706772	40706773	C	T	31	GENIC	possibly homozygous	115374217
6	40707165	40707166	C	T	19	GENIC	homozygous	115205532
6	40707475	40707476	G	T	15	GENIC	homozygous	114767397
6	40707496	40707497	T	G	16	GENIC	homozygous	115205533
6	40707995	40707996	G	A	15	GENIC	homozygous	114767405
6	40708791	40708792	A	G	25	GENIC	homozygous	114767411
6	40709143	40709144	T	A	34	GENIC	homozygous	114767413
6	40709153	40709154	T	G	31	GENIC	homozygous	114767415
6	40709880	40709881	G	A	31	GENIC	homozygous	114767425
6	40709941	40709942	A	G	29	GENIC	homozygous	115374219
6	40710134	40710135	G	A	28	GENIC	homozygous	115374221
6	40711664	40711665	C	G	19	GENIC	homozygous	115374223
6	40713315	40713316	T	C	18	GENIC	homozygous	114767439
6	40713338	40713339	G	A	18	GENIC	homozygous	114767441