chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	47904409	47904410	C	T	68	GENIC	homozygous	115487128
12	47904428	47904429	A	G	69	GENIC	homozygous	115344992
12	47905039	47905040	G	C	49	GENIC	homozygous	115344994
12	47905289	47905290	G	T	44	GENIC	homozygous	115487129
12	47905924	47905925	T	C	62	GENIC	homozygous	115344998
12	47907186	47907187	T	C	67	GENIC	homozygous	115345000
12	47907550	47907551	A	G	60	GENIC	homozygous	115345004
12	47908182	47908183	T	C	58	GENIC	possibly homozygous	115345008
12	47908531	47908532	C	T	54	GENIC	homozygous	115345010
12	47909783	47909784	G	T	52	GENIC	homozygous	115345012
12	47910407	47910408	C	T	58	GENIC	homozygous	115487131
12	47911952	47911953	A	G	65	GENIC	homozygous	115398531
12	47908935	47908935		T	26	GENIC	homozygous	128997847
12	47911418	47911420	AG		41	GENIC	homozygous	128997851
12	47908930	47908931	C	T	28	GENIC	homozygous	115583652
12	47912110	47912111	G	A	65	GENIC	homozygous	115345020
12	47912142	47912143	A	G	64	GENIC	homozygous	115345022
12	47912153	47912154	A	G	61	GENIC	homozygous	115398533
12	47912332	47912333	A	G	46	GENIC	homozygous	115398535
12	47912338	47912339	C	T	47	GENIC	homozygous	115345024
12	47912863	47912864	A	G	44	GENIC	homozygous	115487132
12	47913298	47913299	T	C	52	GENIC	homozygous	115345032
12	47913964	47913965	C	A	70	GENIC	homozygous	115345036
12	47914995	47915001	TTTTTT		40	GENIC	homozygous	128997854
12	47915391	47915392	T	C	67	GENIC	homozygous	115345042
12	47912429	47912429		A	39	GENIC	homozygous	133010404
12	47913636	47913636		T	52	GENIC	possibly homozygous	133010405
12	47919163	47919163		C	61	GENIC	homozygous	128997857
12	47919331	47919338	AGCATGT		50	GENIC	homozygous	128997858