#Novel EM disease candidate genes along with their co-expression status. 
#We also provide the phenotype MIM number and the association with neurological dysfunction (if present) for 8 of these that had been associated with Mendelian phenotypes in OMIM at the time of publication.


gene_name,coexpression_status,omim_Jan_2019
PRDM1,not coexpressed,
WHSC1,coexpressed,
WHSC1L1,highly coexpressed,
PRDM14,NA,
PRDM11,not coexpressed,
PRDM10,coexpressed,
JARID2,coexpressed,
KAT8,not coexpressed,
KAT7,coexpressed,
HDAC1,not coexpressed,
HDAC4,coexpressed,
HDAC2,coexpressed,
HDAC5,not coexpressed,
HDAC3,not coexpressed,
HDAC9,not coexpressed,
HDAC7,coexpressed,
SIRT1,coexpressed,
MTA1,coexpressed,
PBRM1,highly coexpressed,
MTA2,highly coexpressed,
BAHD1,highly coexpressed,
TNRC18,highly coexpressed,
CHD3,not coexpressed,618205(neurological dysfunction)
CBX8,not coexpressed,
MPHOSPH8,highly coexpressed,
CHD9,highly coexpressed,
CHD5,not coexpressed,
CBX1,not coexpressed,
CHD6,highly coexpressed,
CDYL,not coexpressed,
CHD1,coexpressed,617682(neurological dysfunction)
L3MBTL3,not coexpressed,
SFMBT1,not coexpressed,
SFMBT2,not coexpressed,
MBTD1,highly coexpressed,
TRIM28,coexpressed,
TRIM24,not coexpressed,
BPTF,highly coexpressed,617755(neurological dysfunction)
UHRF2,coexpressed,
TRIM33,highly coexpressed,
BAZ1B,highly coexpressed,
MLLT10,coexpressed,
MLLT6,highly coexpressed,
ASXL2,highly coexpressed,617190(neurological dysfunction)
BAZ2B,coexpressed,
BAZ2A,highly coexpressed,
BAZ1A,not coexpressed,
BRPF3,highly coexpressed,
BRPF1,highly coexpressed,617333(neurological dysfunction)
BRD1,highly coexpressed,
CXXC1,coexpressed,
DIDO1,highly coexpressed,
DPF1,NA,
FBXL19,highly coexpressed,
ING3,not coexpressed,
JADE2,coexpressed,
JADE1,not coexpressed,
MTF2,highly coexpressed,
PHF20L1,not coexpressed,
PHF21B,NA,
PHRF1,highly coexpressed,
PHF19,not coexpressed,
PHF23,coexpressed,
PHF12,highly coexpressed,
PHF21A,coexpressed,
PHF13,coexpressed,
PHF1,coexpressed,
PHF3,coexpressed,
PHF20,coexpressed,
ZMYND8,coexpressed,
PYGO2,coexpressed,
PYGO1,not coexpressed,
DPF2,coexpressed,618027(neurological dysfunction)
RSF1,highly coexpressed,
TAF3,highly coexpressed,
PSIP1,highly coexpressed,
GLYR1,highly coexpressed,
HDGFRP3,coexpressed,
PWWP2A,not coexpressed,
SND1,not coexpressed,
TDRD1,NA,
RNF17,NA,
TDRD5,NA,
MORC3,coexpressed,
KAT2B,coexpressed,
BRD4,highly coexpressed,
BRD7,coexpressed,
BRD2,highly coexpressed,
ATAD2B,coexpressed,
ATAD2,not coexpressed,
BRWD1,highly coexpressed,
PHIP,coexpressed,617991(neurological dysfunction)
MBD1,highly coexpressed,
MBD3,coexpressed,
MBD2,not coexpressed,
MBD6,highly coexpressed,
TET1,not coexpressed,
TET3,coexpressed,
SMARCA5,coexpressed,
EED,not coexpressed,617561(neurological dysfunction)
INO80,highly coexpressed,
EP400,highly coexpressed,