| HOXA@ |
|
homeobox A cluster
|
|
|
0.599 |
0.654 |
| H3P47 |
|
H3 histone pseudogene 47
|
|
|
0.603 |
0.538 |
| SEA |
|
S13 erythroblastosis (avian) oncogene homolog
|
|
|
0.606 |
0.615 |
| HOXD@ |
|
homeobox D cluster
|
|
|
0.631 |
0.538 |
| HOXB@ |
|
homeobox B cluster
|
|
|
0.631 |
0.538 |
| DGCR |
|
DiGeorge syndrome chromosome region
|
|
|
0.678 |
0.538 |
| MIR876 |
|
microRNA 876
|
|
|
0.666 |
0.385 |
| HOXC@ |
|
homeobox C cluster
|
|
|
0.695 |
0.462 |
| DEL11P13 |
|
Wilms tumor, aniridia, genitourinary anomalies and mental retardation syndrome
|
|
|
0.716 |
0.538 |
| MIR595 |
|
microRNA 595
|
|
|
0.722 |
0.346 |
| HFM |
|
Hemifacial microsomia
|
|
|
0.722 |
0.385 |
| ZRS |
|
ZPA regulatory sequence
|
|
|
0.722 |
0.269 |
| IH |
|
Hemihypertrophy
|
|
|
0.751 |
0.385 |
| SHFM3 |
|
Split-hand/foot malformation 3
|
|
|
0.780 |
0.115 |
| AFA |
|
ankyloblepharon filiforme adnatum
|
|
|
0.792 |
0.462 |
| FECD3 |
|
Corneal dystrophy, Fuchs endothelial, 3
|
|
|
0.769 |
0.385 |
| GLC3B |
|
glaucoma 3, primary infantile, B
|
|
|
0.769 |
0.154 |
| RRDX |
|
Radial ray deficiency
|
|
|
0.805 |
0.154 |
| PUJO |
|
pelviureteric junction obstruction
|
|
|
0.821 |
0.154 |
| ERVMER61-1 |
|
endogenous retrovirus group MER61 member 1
|
|
|
0.890 |
0.115 |
| OFC2 |
|
orofacial cleft 2
|
|
|
0.931 |
0.115 |
| SHFL1 |
|
Split-hand/foot malformation with long bone deficiency 1
|
|
|
1.000 |
0.038 |
| MACOM |
|
macrophthalmia, colobomatous, with microcornea
|
|
|
1.000 |
0.077 |
| PTLAH |
|
patella aplasia-hypoplasia
|
|
|
0.931 |
0.115 |
| GLC3C |
|
glaucoma 3, primary congenital, C
|
|
|
1.000 |
0.115 |