chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	41700021	41700022	T		26	GENIC	homozygous	129046393
13	41700033	41700034	G	A	23	GENIC	homozygous	118449092
13	41700064	41700065	A		18	GENIC	homozygous	129046394
13	41700088	41700090	CC		17	GENIC	homozygous	129046395
13	41700150	41700152	AG		9	GENIC	homozygous	130416948
13	41700183	41700184	G		9	GENIC	homozygous	130416949
13	41700694	41700695	A		7	GENIC	homozygous	129046396
13	41700709	41700710	C	A	14	GENIC	homozygous	118449093
13	41700712	41700712		C	14	GENIC	homozygous	129046397
13	41700724	41700725	C		15	GENIC	homozygous	129046398
13	41700728	41700729	G		15	GENIC	homozygous	129046399
13	41700735	41700736	A		15	GENIC	homozygous	129046400
13	41700745	41700746	C		16	GENIC	homozygous	129046401
13	41700758	41700759	C		18	GENIC	homozygous	129046402
13	41700762	41700763	A		19	GENIC	homozygous	129046403
13	41700753	41700754	T	C	17	GENIC	homozygous	114719433
13	41700776	41700777	C		22	GENIC	homozygous	129046404
13	41700786	41700787	A		23	GENIC	homozygous	129046405
13	41700788	41700789	A		23	GENIC	homozygous	129046406
13	41701432	41701432		C	13	GENIC	heterozygous	133016441
13	41701514	41701514		A	18	GENIC	possibly homozygous	129046407
13	41713174	41713175	C		59	GENIC	homozygous	129046412
13	41713193	41713194	C		61	GENIC	homozygous	129046413
13	41713207	41713208	G		60	GENIC	homozygous	129046414
13	41701432	41701433	T	C	13	GENIC	heterozygous	114719435
13	41700754	41700755	G	T	17	GENIC	homozygous	114857334
13	41700782	41700783	T	A	22	GENIC	homozygous	114857336
13	41712422	41712423	G	T	18	GENIC	heterozygous	130422184
13	41712423	41712424	G	T	18	GENIC	heterozygous	130692394