chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	126337430	126337431	C	G	48	GENIC	homozygous	111698435
3	126338925	126338926	C	T	51	GENIC	homozygous	111698437
3	126339137	126339138	C	T	55	GENIC	homozygous	111698439
3	126339494	126339495	T	C	49	GENIC	homozygous	111698441
3	126339999	126340000	C	T	48	GENIC	homozygous	111698443
3	126340270	126340271	T	C	40	GENIC	homozygous	111698447
3	126340519	126340520	T	C	31	GENIC	homozygous	111698449
3	126340967	126340968	C	G	29	GENIC	homozygous	111698451
3	126339124	126339125	A		55	GENIC	homozygous	127927374
3	126340483	126340483		A	31	GENIC	possibly homozygous	127927375
3	126339554	126339555	G	A	44	GENIC	homozygous	112299275
3	126339764	126339765	T	C	55	GENIC	homozygous	112299277
3	126341288	126341288		G	2	GENIC	homozygous	127927376
3	126341318	126341319	G	A	6	GENIC	homozygous	129898756
3	126341338	126341338		C	12	GENIC	homozygous	127927377
3	126341405	126341406	T		28	GENIC	homozygous	127927383
3	126341344	126341345	T		16	GENIC	homozygous	127927378
3	126341351	126341351		G	17	GENIC	homozygous	127927379
3	126341360	126341361	C		18	GENIC	homozygous	127927380
3	126341366	126341367	T		18	GENIC	homozygous	127927381
3	126341374	126341374		T	21	GENIC	homozygous	127927382
3	126341294	126341301	AGGCGGA		3	GENIC	homozygous	134001501
3	126341321	126341323	GC		7	GENIC	homozygous	129891479
3	126341413	126341413		TGGG	31	GENIC	homozygous	127927384
3	126341952	126341953	C	G	41	GENIC	homozygous	111698465
3	126342255	126342256	A	G	54	GENIC	homozygous	111698467
3	126343025	126343026	T	C	52	GENIC	homozygous	111698469
3	126343707	126343708	A	G	32	GENIC	homozygous	112299279
3	126344828	126344828		A	46	GENIC	homozygous	127927385
3	126345954	126345955	G		44	GENIC	homozygous	130910642
3	126341719	126341719		C	38	GENIC	homozygous	130910641