chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	90534112	90534113	G	A	31	GENIC	homozygous	114574561
13	90534836	90534837	G	T	23	GENIC	homozygous	114725326
13	90534844	90534845	T	G	20	GENIC	homozygous	114693396
13	90535360	90535361	C	T	34	GENIC	possibly homozygous	115014844
13	90539779	90539780	A	G	36	GENIC	possibly homozygous	114693398
13	90540914	90540915	T	C	26	GENIC	homozygous	114574567
13	90541226	90541227	T	C	27	GENIC	homozygous	114574569
13	90549803	90549804	C	T	28	GENIC	possibly homozygous	115014846
13	90552530	90552531	A	T	28	GENIC	homozygous	114574587
13	90554661	90554662	T	G	23	GENIC	homozygous	114574591
13	90555633	90555634	G	A	26	GENIC	homozygous	114574595
13	90556520	90556521	C	T	36	GENIC	possibly homozygous	115014848
13	90569066	90569067	T	C	29	GENIC	homozygous	114574611
13	90569133	90569134	C	T	26	GENIC	homozygous	114574619
13	90570809	90570810	T	A	28	GENIC	homozygous	114574621
13	90573390	90573391	G	A	30	GENIC	possibly homozygous	115014850
13	90574780	90574781	C	T	26	GENIC	possibly homozygous	115014852
13	90579656	90579657	T	C	31	GENIC	homozygous	114574632
13	90579806	90579807	T	A	30	GENIC	homozygous	114693400
13	90580402	90580403	T	C	35	GENIC	homozygous	114574634
13	90581577	90581578	G	A	21	GENIC	possibly homozygous	115014856
13	90586693	90586694	G	A	37	GENIC	homozygous	115014858
13	90586893	90586894	C	T	25	GENIC	possibly homozygous	115014860
13	90586918	90586919	A	G	23	GENIC	homozygous	114574644