chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
15	31674494	31674495	G		13	GENIC	homozygous	139626328
15	31681016	31681017	T		20	GENIC	homozygous	139626329
15	31683940	31683940		A	19	GENIC	homozygous	139626330
15	31685509	31685509		G	19	GENIC	homozygous	139626331
15	31687668	31687668		A	35	GENIC	homozygous	139626332
15	31687705	31687706	T		35	GENIC	homozygous	139626333
15	31687738	31687738		T	30	GENIC	homozygous	139626334
15	31687982	31687983	C		26	GENIC	homozygous	139626335
15	31688005	31688006	T	A	26	GENIC	possibly homozygous	139709030
15	31688064	31688064		C	25	GENIC	homozygous	139626336
15	31688084	31688085	C		24	GENIC	homozygous	139626337
15	31688119	31688119		C	29	GENIC	homozygous	139626338
15	31688217	31688217		A	25	GENIC	homozygous	139626339
15	31688232	31688233	T		23	GENIC	homozygous	139626340
15	31688240	31688241	G		23	GENIC	homozygous	139626341
15	31688368	31688370	AC		21	GENIC	homozygous	139626342
15	31688385	31688385		C	21	GENIC	homozygous	139626343
15	31688488	31688488		G	29	GENIC	homozygous	139626344
15	31688515	31688517	AT		29	GENIC	homozygous	139626345
15	31688655	31688655		C	20	GENIC	homozygous	139626346
15	31688756	31688757	C		21	GENIC	homozygous	139626347
15	31688839	31688840	G		18	GENIC	homozygous	139626348