chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	31694654	31694655	T	C	33	GENIC	homozygous	115812390
11	31694813	31694814	G	T	46	GENIC	possibly homozygous	115812392
11	31695708	31695709	A	G	21	GENIC	homozygous	115812394
11	31696294	31696295	C	G	37	GENIC	homozygous	115812396
11	31696938	31696939	A	C	42	GENIC	homozygous	115812398
11	31697393	31697394	A	G	36	GENIC	homozygous	115812400
11	31698450	31698451	A	G	52	GENIC	homozygous	115812402
11	31699233	31699234	A	G	37	GENIC	homozygous	115812404
11	31700631	31700632	T	C	60	GENIC	homozygous	115812406
11	31700713	31700714	C	G	43	GENIC	homozygous	115812408
11	31701245	31701246	A	G	46	GENIC	homozygous	115812410
11	31701336	31701337	C	G	47	GENIC	homozygous	115812412
11	31701579	31701580	A	G	33	GENIC	homozygous	115812414
11	31702613	31702614	T	C	43	GENIC	homozygous	115812416
11	31702797	31702798	C	T	55	GENIC	possibly homozygous	115812418
11	31702916	31702917	T	C	38	GENIC	homozygous	115812420
11	31704949	31704950	C	T	52	GENIC	possibly homozygous	115812422
11	31705451	31705452	A	G	60	GENIC	homozygous	115812424
11	31705705	31705706	G	A	35	GENIC	homozygous	115812426
11	31705720	31705721	C	A	33	GENIC	homozygous	115812428
11	31706330	31706331	G	A	58	GENIC	homozygous	115812430
11	31706697	31706698	T	A	36	GENIC	homozygous	115812432
11	31707184	31707185	G	A	60	GENIC	homozygous	115960357
11	31707201	31707202	T	A	58	GENIC	possibly homozygous	115960358
11	31707502	31707503	A	C	66	GENIC	homozygous	115812434
11	31707517	31707518	C	T	65	GENIC	homozygous	115812436
11	31707595	31707596	G	A	60	GENIC	homozygous	115812438
11	31708283	31708284	C	T	63	GENIC	homozygous	115812440
11	31709305	31709306	G	T	44	GENIC	homozygous	115812442
11	31710094	31710095	G	A	39	GENIC	homozygous	115812444
11	31710955	31710956	G	A	41	GENIC	homozygous	115812446
11	31711629	31711630	T	A	36	GENIC	homozygous	115812448
11	31712089	31712090	G	A	36	GENIC	possibly homozygous	115960360
11	31712301	31712302	A	G	37	GENIC	homozygous	115812450