| AMD1P2 |
|
adenosylmethionine decarboxylase 1 pseudogene 2
|
|
|
0.608 |
0.538 |
| ANCR |
|
Angelman syndrome chromosome region
|
|
|
0.751 |
0.154 |
| APOC1P1 |
|
apolipoprotein C1 pseudogene 1
|
|
|
0.890 |
0.154 |
| ATHS |
|
atherosclerosis susceptibility (lipoprotein associated)
|
|
|
0.551 |
0.769 |
| BCYRN1 |
|
brain cytoplasmic RNA 1
|
|
|
0.666 |
0.423 |
| BTF3P11 |
|
basic transcription factor 3 pseudogene 11
|
|
|
0.519 |
0.731 |
| CCT |
|
cataract, congenital, total
|
|
|
0.588 |
0.769 |
| CTAA1 |
|
cataract, anterior polar 1
|
|
|
0.568 |
0.731 |
| EEF1B2P2 |
|
eukaryotic translation elongation factor 1 beta 2 pseudogene 2
|
|
|
0.612 |
0.577 |
| FKBP1AP1 |
|
FKBP prolyl isomerase 1A pseudogene 1
|
|
|
0.700 |
0.538 |
| FKBP1AP2 |
|
FKBP prolyl isomerase 1A pseudogene 2
|
|
|
0.700 |
0.538 |
| FKBP1AP3 |
|
FKBP prolyl isomerase 1A pseudogene 3
|
|
|
0.700 |
0.538 |
| FKBP1AP4 |
|
FKBP prolyl isomerase 1A pseudogene 4
|
|
|
0.700 |
0.538 |
| FRA6E |
|
fragile site, aphidicolin type, common, fra(6)(q26)
|
|
|
0.792 |
0.231 |
| FRA7G |
|
fragile site, aphidicolin type, common, fra(7)(q31.2)
|
|
|
0.695 |
0.462 |
| FRA16D |
|
fragile site, aphidicolin type, common, fra(16)(q23.2)
|
|
|
0.656 |
0.577 |
| FTH1P3 |
|
ferritin heavy chain 1 pseudogene 3
|
|
|
0.751 |
0.269 |
| GCY |
|
growth control, Y chromosome influenced
|
|
|
0.631 |
0.615 |
| HOXA@ |
|
homeobox A cluster
|
|
|
0.599 |
0.654 |
| HOXD@ |
|
homeobox D cluster
|
|
|
0.631 |
0.538 |
| HTC2 |
|
hypertrichosis 2 (generalized, congenital)
|
|
|
0.392 |
0.808 |
| IFN1@ |
|
interferon, type 1, cluster
|
|
|
0.565 |
0.731 |
| MT1JP |
|
metallothionein 1J, pseudogene
|
|
|
0.588 |
0.731 |
| NM |
|
neutrophil migration
|
|
|
0.473 |
0.808 |
| PKD3 |
|
polycystic kidney disease 3 (autosomal dominant)
|
|
|
0.760 |
0.308 |