Table 3.

Genes located in regions capable of forming highly stable secondary structures and disease associations

Gene	Chromosomal position	Fragile site	Insertion, deletion, translocationa	Point mutationa
PHYH	10p13			+
NMT2	10p13		+
VIM	10p13			+
CACNB2	10p12.33			+
NEBL	10p12.31		+
BMI1	10p12.2			+
PTF1A	10p12.2			+
MAP3K8	10p11.23			+
ZEB1	10p11.22			+
RET	10q11.21	FRA10G	+	+
CXCL12	10q11.21	FRA10G		+
ALOX5	10q11.21	FRA10G		+
CHAT	10q11.23	FRA10G		+
CCDC6	10q21.2	FRA10C	+
RHOBTB1	10q21.2	FRA10C		+
STOX1	10q21.3	FRA10C		+
HK1	10q22.1	FRA10D	+
NEUROG3	10q22.1	FRA10D		+
PCBD1	10q22.1	FRA10D		+
CDH23	10q22.1	FRA10D		+
CHST3	10q22.1	FRA10D		+
KCNMA1	10q22.3			+
ZMIZ1	10q22.3		+
CDHR1	10q23.1			+
LDB3	10q23.2			+
BMPR1A	10q23.2		+	+
GLUD1	10q23.2			+
PTEN	10q23.31	FRA10A	+	+
RBP4	10q23.33	FRA10A		+
HPS1	10q24.2	FRA10A	+
ABCC2	10q24.2	FRA10A	+	+
PAX2	10q24.31		+	+
PDZD7	10q24.31		+
FGF8	10q24.32			+
HPS6	10q24.32		+	+
PITX3	10q24.32		+	+
NFKB2	10q24.32		+
CNNM2	10q24.32		+	+
COL17A1	10q24.33		+	+
ADD3	10q25.1		+
ADRB1	10q25.3		+	+
BAG3	10q26.11	FRA10F	+	+
FGFR2	10q26.13	FRA10F	+	+
PLEKHA1	10q26.13	FRA10F		+
HTRA1	10q26.13	FRA10F		+
OAT	10q26.13	FRA10F	+	+
ADAM12	10q26.2			+

^aDetailed descriptions of diseases and references are found in Supplementary Material, Table S5.