H3P10 |
|
H3 histone pseudogene 10
|
|
|
0.350 |
0.846 |
HTC2 |
|
hypertrichosis 2 (generalized, congenital)
|
|
|
0.392 |
0.808 |
PECAM1 |
P16284
|
platelet and endothelial cell adhesion molecule 1
|
Cell adhesion
|
|
0.426 |
0.846 |
IFNA2 |
P01563
|
interferon alpha 2
|
|
|
0.442 |
0.885 |
SRY |
Q05066
|
sex determining region Y
|
Transcription factor
|
|
0.456 |
0.808 |
IGH |
|
immunoglobulin heavy locus
|
|
|
0.473 |
0.654 |
MIR92B |
|
microRNA 92b
|
|
|
0.590 |
0.654 |
TMED10P1 |
|
transmembrane p24 trafficking protein 10 pseudogene 1
|
|
|
0.663 |
0.615 |
H3P17 |
|
H3 histone pseudogene 17
|
|
|
0.674 |
0.615 |
DGCR |
|
DiGeorge syndrome chromosome region
|
|
|
0.678 |
0.538 |
CLLS2 |
|
Disrupted in B-cell neoplasia
|
|
|
0.678 |
0.346 |
FRA7G |
|
fragile site, aphidicolin type, common, fra(7)(q31.2)
|
|
|
0.695 |
0.462 |
MIR595 |
|
microRNA 595
|
|
|
0.722 |
0.346 |
MLSM7 |
|
Myelodysplasia and leukemia syndrome with monosomy 7
|
|
|
0.743 |
0.192 |
HLA-J |
|
major histocompatibility complex, class I, J (pseudogene)
|
|
|
0.861 |
0.269 |
DFNB20 |
|
deafness, autosomal recessive 20
|
|
|
1.000 |
0.115 |
TET2 |
Q6N021
|
tet methylcytosine dioxygenase 2
|
|
4.3E-54 |
0.458 |
0.808 |
SAMD9 |
Q5K651
|
sterile alpha motif domain containing 9
|
|
1.1E-33 |
0.606 |
0.808 |
IL3RA |
P26951
|
interleukin 3 receptor subunit alpha
|
Signaling
|
3.0E-27 |
0.560 |
0.769 |
EVPL |
Q92817
|
envoplakin
|
Cellular structure
|
5.7E-25 |
0.599 |
0.423 |
EGF |
P01133
|
epidermal growth factor
|
|
8.5E-17 |
0.357 |
0.923 |
SLC12A9 |
Q9BXP2
|
solute carrier family 12 member 9
|
Transporter
|
1.2E-15 |
0.454 |
0.769 |
SAMD9L |
Q8IVG5
|
sterile alpha motif domain containing 9 like
|
|
5.6E-15 |
0.700 |
0.500 |
MPO |
P05164
|
myeloperoxidase
|
Enzyme
|
7.1E-15 |
0.377 |
0.923 |
ASXL1 |
Q8IXJ9
|
ASXL transcriptional regulator 1
|
|
1.3E-14 |
0.482 |
0.808 |