Table 1.

Non-syndromic hearing loss loci (dominant DFNA, recessive DFNB and X-linked DFNX) for which no causative gene has been identified. We present here the number of genes expressed in the inner ear in each locus (i.e FPKM>1 in at least 1 sample).

Locus Name	Chr	Locus start	Locus End	Locus size (Mb)	N annotated genes in locus	N expressed genes (FPKM >1)
DFNB96	1	5400000	20400000	15.0	386	119
DFNA7	1	142600000	165500000	22.9	852	282
DFNB45	1	236600000	249250621	12.7	232	45
DFNB47	2	7100000	16700000	9.6	138	35
DFNA43	2	75000000	83300000	8.3	74	11
DFNA16	2	148700000	169700000	21.0	200	64
DFNA18	3	129200000	138700000	9.5	150	49
DFNA27	4	52700000	66600000	13.9	155	38
DFNA52	4	123800000	139500000	15.7	127	23
DFNA24	4	183200000	191154296	8.0	153	37
DFNA21	6	11600000	25200000	13.6	162	53
DFNB38	6	161000000	171115067	10.1	128	25
DFNB44	7	37200000	72200000	35.0	571	108
DFNB14	7	107400000	127100000	19.7	189	49
DFNB13	7	138200000	159138663	20.9	442	122
DFNB71	8	12700000	23300000	10.6	159	55
DFNA47	9	14200000	33200000	19.0	210	52
DFNA59	11	26100000	63400000	37.3	783	193
DFNB51	11	31000000	43500000	12.5	136	44
DFNB20	11	130800000	135006516	4.2	47	12
DFNB62	12	10100000	27800000	17.7	281	97
DFNA53	14	19100000	33300000	14.2	519	122
DFNB85	17	10700000	31800000	21.1	639	174
DFNB46	18	0	7100000	7.1	132	33
DFNB68	19	6900000	13900000	7.0	349	126
DFNB65	20	49800000	63025520	13.2	249	61
DFNB40	22	17900000	29600000	11.7	490	100
DFNX3	X	29300000	61500000	32.2	23	5
DFNX5	X	108700000	147100000	38.4	537	95