chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	38433174	38433175	A	G	13	GENIC	homozygous	46117258
19	38433282	38433283	G	-	5	GENIC	homozygous	46117259
19	38433294	38433295	A	G	4	GENIC	homozygous	46117260
19	38433385	38433386	T	A	4	GENIC	homozygous	46117261
19	38435137	38435138	T	TA	19	GENIC	homozygous	46117262
19	38435656	38435657	C	T	18	GENIC	homozygous	46117263
19	38436271	38436272	G	A	23	GENIC	possibly homozygous	46117264
19	38438037	38438038	C	CT	7	GENIC	heterozygous	46251271
19	38438554	38438555	G	C	17	GENIC	homozygous	46117265
19	38438555	38438556	T	C	17	GENIC	homozygous	46117266
19	38438911	38438912	T	C	44	GENIC	homozygous	46117267
19	38438912	38438913	T	C	44	GENIC	homozygous	46117268
19	38439655	38439656	C	T	13	GENIC	homozygous	46117269
19	38440526	38440530	CCCC	----	8	GENIC	possibly homozygous	46117270
19	38440928	38440929	T	TTTGTTGTTG	17	GENIC	homozygous	46117271
19	38441771	38441772	A	AGTGT	1	GENIC	homozygous	46251272
19	38441803	38441804	T	-	5	GENIC	homozygous	46117274
19	38443782	38443783	A	T	18	GENIC	homozygous	46117275
19	38444423	38444429	TGCTGC	------	16	GENIC	homozygous	46117276
19	38447995	38447996	A	G	13	GENIC	homozygous	46117277
19	38448032	38448033	G	GA	12	GENIC	homozygous	46117278
19	38448050	38448051	G	GA	14	GENIC	homozygous	46117279
19	38448703	38448704	T	G	13	GENIC	heterozygous	46117280
19	38451401	38451402	T	C	12	GENIC	homozygous	46117282
19	38452010	38452011	C	CT	4	GENIC	heterozygous	46117283
19	38454269	38454272	CCC	---	3	GENIC	homozygous	46117284
19	38456077	38456078	A	AGTGTGTGT	3	GENIC	homozygous	46117285
19	38456965	38456966	T	TTA	19	GENIC	homozygous	46117287
19	38459508	38459509	T	C	24	GENIC	homozygous	46117288
19	38459848	38459857	GTTTCCCCG	---------	11	GENIC	homozygous	46117289
19	38460344	38460345	A	-	3	GENIC	homozygous	46117291
19	38460851	38460852	A	T	11	GENIC	homozygous	46117292
19	38461496	38461497	T	C	31	GENIC	homozygous	46117293
19	38440928	38440929	T	G	29	GENIC	heterozygous	46210884