chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
15	51385666	51385667	C	T	47	GENIC	homozygous	112507172
15	51386648	51386649	A	G	60	GENIC	possibly homozygous	112507174
15	51388697	51388698	C	T	59	GENIC	homozygous	112507176
15	51388931	51388932	G	A	60	GENIC	homozygous	112507179
15	51389531	51389532	G	C	46	GENIC	homozygous	112507181
15	51389550	51389551	G	C	47	GENIC	homozygous	112507183
15	51390350	51390351	C	T	42	GENIC	homozygous	112507185
15	51393541	51393541		CAAAGATGCATATGCACAGATCTAG	46	GENIC	homozygous	129255656
15	51390747	51390748	A		48	GENIC	homozygous	129255654
15	51393170	51393172	AT		37	GENIC	possibly homozygous	129255655
15	51393657	51393658	G	C	48	GENIC	homozygous	112507187
15	51393803	51393804	T	C	69	GENIC	homozygous	112507189
15	51393867	51393868	G	A	70	GENIC	homozygous	112507191
15	51394484	51394485	G	A	52	GENIC	homozygous	112507193
15	51394490	51394491	A	G	57	GENIC	homozygous	112507195
15	51394753	51394759	TGTCTG		29	GENIC	homozygous	129255657
15	51397581	51397582	G	A	57	GENIC	homozygous	112507199
15	51394782	51394783	C	G	24	GENIC	homozygous	124076419
15	51396215	51396216	G	A	68	GENIC	homozygous	112507197
15	51394770	51394771	C	G	26	GENIC	homozygous	129316734
15	51394772	51394773	C	G	26	GENIC	homozygous	129316735
15	51394774	51394775	C	G	26	GENIC	homozygous	129316736
15	51394776	51394777	C	G	24	GENIC	homozygous	129316737
15	51394778	51394779	C	G	24	GENIC	homozygous	129316738
15	51394780	51394781	C	G	24	GENIC	homozygous	129316739
15	51397663	51397664	C	A	42	GENIC	homozygous	112507201
15	51398530	51398531	C	T	57	GENIC	homozygous	112507203
15	51399702	51399705	TTC		40	GENIC	homozygous	129255658
15	51399706	51399707	G		41	GENIC	homozygous	129255659
15	51399708	51399709	G	A	42	GENIC	homozygous	112507205
15	51398141	51398142	A		43	GENIC	heterozygous	130592670