chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	51022996	51022997	G	A	29	GENIC	homozygous	114672241
13	51023064	51023065	T	G	24	GENIC	homozygous	115100753
13	51023591	51023592	T	C	28	GENIC	homozygous	114672243
13	51024246	51024247	C	T	50	GENIC	homozygous	114672245
13	51023188	51023189	A		41	GENIC	homozygous	131126449
13	51023347	51023348	G	A	16	GENIC	homozygous	114890393
13	51023882	51023883	T	G	45	GENIC	homozygous	114890395
13	51024301	51024302	A	G	46	GENIC	homozygous	114890397
13	51024302	51024303	C	T	45	GENIC	homozygous	114890399
13	51024523	51024524	C	T	54	GENIC	homozygous	114890401
13	51024772	51024773	A		50	GENIC	homozygous	131126450
13	51024773	51024774	C	T	51	GENIC	homozygous	114890403
13	51025241	51025242	A	T	49	GENIC	homozygous	114342375
13	51024364	51024365	T	C	46	GENIC	homozygous	114342371
13	51023783	51023784	G	T	41	GENIC	homozygous	114342369
13	51025424	51025425	G	C	31	GENIC	homozygous	114890405
13	51026234	51026235	A	G	41	GENIC	homozygous	114890407
13	51026402	51026403	G	A	39	GENIC	homozygous	114342377
13	51026717	51026718	C		47	GENIC	homozygous	131126451
13	51026928	51026929	T	C	49	GENIC	homozygous	114890409
13	51027012	51027013	T	C	34	GENIC	homozygous	114890411
13	51027431	51027432	G	A	46	GENIC	homozygous	114342379
13	51028237	51028238	A	T	45	GENIC	homozygous	114672249
13	51028446	51028447	C	A	31	GENIC	possibly homozygous	114890413
13	51028743	51028744	C	T	45	GENIC	possibly homozygous	114890415
13	51029139	51029140	C	G	41	GENIC	homozygous	114890417
13	51029367	51029368	A	T	45	GENIC	homozygous	114342381
13	51029598	51029599	G	A	51	GENIC	homozygous	114890419
13	51029669	51029670	A	G	62	GENIC	homozygous	114342383
13	51029870	51029871	A	G	45	GENIC	homozygous	114342387
13	51030147	51030148	C	G	46	GENIC	homozygous	114890421
13	51030402	51030403	C	T	51	GENIC	homozygous	114890423
13	51030556	51030557	T	C	48	GENIC	homozygous	114342389
13	51030613	51030613		AC	38	GENIC	homozygous	131126452
13	51028085	51028086	G	A	38	GENIC	homozygous	114948043