chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	93386518	93386519	A	C	7	GENIC	heterozygous	115072229
6	93386980	93386981	T	A	3	GENIC	heterozygous	126402960
6	93391448	93391449	T	C	4	GENIC	homozygous	114903337
6	93391669	93391670	C	A	18	GENIC	homozygous	114903339
6	93393417	93393418	C	T	8	GENIC	homozygous	114903341
6	93393565	93393566	A	T	13	GENIC	homozygous	114903343
6	93395012	93395013	C	T	11	GENIC	homozygous	114903345
6	93396093	93396094	C	T	16	GENIC	homozygous	114903347
6	93396527	93396528	T	C	28	GENIC	homozygous	114903349
6	93397657	93397658	T	C	11	GENIC	homozygous	114903352
6	93397940	93397941	A	G	32	GENIC	homozygous	114903354
6	93400721	93400722	C	T	14	GENIC	homozygous	114903356
6	93401703	93401704	G	T	29	GENIC	homozygous	114903358
6	93402134	93402135	A	G	8	GENIC	homozygous	114903360
6	93402294	93402295	C	T	11	GENIC	homozygous	114903362
6	93402899	93402900	A	G	17	GENIC	homozygous	114903364
6	93403466	93403467	C	T	22	GENIC	homozygous	114903366
6	93403587	93403588	C	A	7	GENIC	homozygous	114903368
6	93404478	93404479	T	C	13	GENIC	homozygous	114903370
6	93405103	93405104	T	C	16	GENIC	homozygous	114903374
6	93405243	93405244	C	T	22	GENIC	possibly homozygous	114903376
6	93406391	93406392	C	T	9	GENIC	homozygous	114903378
6	93406767	93406768	A	G	6	GENIC	homozygous	114903380
6	93406800	93406801	G	C	8	GENIC	homozygous	114903382
6	93407376	93407377	A	T	16	GENIC	homozygous	114903384
6	93407861	93407862	G	A	21	GENIC	homozygous	114903386
6	93408164	93408165	C	T	27	GENIC	homozygous	114903388
6	93408210	93408211	G	T	24	GENIC	homozygous	114903390
6	93408991	93408992	G	C	12	GENIC	homozygous	114903392
6	93409910	93409911	T	A	5	GENIC	heterozygous	118574711
6	93410582	93410583	C	A	11	GENIC	homozygous	114903394
6	93411358	93411359	C	T	9	GENIC	homozygous	114903396
6	93411361	93411362	C	T	10	GENIC	homozygous	114903398
6	93406772	93406773	G	A	5	GENIC	homozygous	115139373