chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	50286204	50286205	G	A	25	GENIC	homozygous	115403401
12	50287755	50287756	T	A	38	GENIC	homozygous	115351954
12	50289336	50289337	G	A	23	GENIC	homozygous	115403403
12	50291761	50291762	C	T	12	GENIC	homozygous	115403405
12	50292562	50292563	C	A	28	GENIC	homozygous	115403407
12	50292564	50292565	C	G	27	GENIC	homozygous	115403409
12	50293052	50293053	T	C	21	GENIC	homozygous	115403411
12	50293436	50293437	G	A	25	GENIC	homozygous	115403413
12	50299349	50299350	T	G	15	GENIC	homozygous	115403415
12	50299686	50299687	C	A	24	GENIC	homozygous	115403417
12	50300607	50300608	A	T	30	GENIC	homozygous	115351964
12	50306119	50306120	C	T	25	GENIC	homozygous	115403419
12	50306286	50306287	C	T	38	GENIC	homozygous	115403421
12	50306573	50306574	G	A	30	GENIC	homozygous	115351966
12	50307296	50307297	C	T	35	GENIC	homozygous	115403423
12	50309161	50309162	G	A	43	GENIC	homozygous	115403425
12	50311572	50311573	A	G	30	GENIC	homozygous	115403429
12	50314675	50314676	G	A	20	GENIC	homozygous	115403433
12	50305502	50305503	T	C	33	GENIC	homozygous	115496312
12	50307725	50307726	A	G	23	GENIC	homozygous	115506194
12	50311230	50311231	A	G	21	GENIC	homozygous	115506196