chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	54634392	54634393	T	TG	13	GENIC	homozygous	46165145
19	54634446	54634447	G	A	18	GENIC	homozygous	46165146
19	54634453	54634454	A	T	9	GENIC	homozygous	46165147
19	54634473	54634474	G	A	9	GENIC	homozygous	46165148
19	54634485	54634486	G	A	9	GENIC	homozygous	46165149
19	54634492	54634493	C	A	9	GENIC	homozygous	46165150
19	54634635	54634636	G	GATTTATTC	8	GENIC	homozygous	46165152
19	54635294	54635295	C	CAT	20	GENIC	homozygous	46165155
19	54635528	54635529	A	T	11	GENIC	homozygous	46308107
19	54635658	54635659	A	T	13	GENIC	homozygous	46308108
19	54635850	54635856	ACCAAC	------	8	GENIC	homozygous	46308109
19	54638912	54638913	C	T	11	GENIC	homozygous	46308110
19	54641163	54641164	C	T	10	GENIC	homozygous	46308112
19	54641611	54641612	C	T	16	GENIC	homozygous	46308113
19	54641923	54641924	G	GA	11	GENIC	homozygous	46263177
19	54642949	54642950	G	GTGCTACAGT	9	GENIC	homozygous	46308115
19	54643280	54643281	C	T	12	GENIC	homozygous	46165161
19	54650091	54650092	T	C	10	GENIC	homozygous	46165169
19	54652403	54652423	ATATATATACATATATATAT	--------------------	8	GENIC	homozygous	46464102
19	54652452	54652453	A	AAT	15	GENIC	homozygous	46165176
19	54652476	54652478	AT	--	13	GENIC	homozygous	46308117
19	54652776	54652777	G	A	18	GENIC	homozygous	46308118
19	54653910	54653911	A	G	25	GENIC	homozygous	46165183
19	54654577	54654578	T	G	19	GENIC	homozygous	46308119
19	54655269	54655270	C	T	9	GENIC	homozygous	46165184