H3P10 |
|
H3 histone pseudogene 10
|
|
|
0.350 |
0.846 |
MTCO2P12 |
|
MT-CO2 pseudogene 12
|
|
|
0.368 |
0.962 |
HTC2 |
|
hypertrichosis 2 (generalized, congenital)
|
|
|
0.392 |
0.808 |
TERC |
|
telomerase RNA component
|
|
|
0.471 |
0.846 |
PWAR1 |
|
Prader Willi/Angelman region RNA 1
|
|
|
0.490 |
0.769 |
H19 |
|
H19 imprinted maternally expressed transcript
|
|
|
0.494 |
0.923 |
RNU4ATAC |
|
RNA, U4atac small nuclear (U12-dependent splicing)
|
|
|
0.556 |
0.808 |
TRNS1 |
|
tRNA
|
|
|
0.555 |
0.808 |
XIST |
|
X inactive specific transcript
|
|
|
0.522 |
0.808 |
H3P8 |
|
H3 histone pseudogene 8
|
|
|
0.544 |
0.808 |
IFN1@ |
|
interferon, type 1, cluster
|
|
|
0.565 |
0.731 |
RSS |
|
Russell Silver syndrome
|
|
|
0.578 |
0.692 |
NPHP3-ACAD11 |
|
NPHP3-ACAD11 readthrough (NMD candidate)
|
|
|
0.663 |
0.577 |
WHCR |
|
Wolf-Hirschhorn syndrome chromosome region
|
|
|
0.638 |
0.577 |
PWRN1 |
|
Prader-Willi region non-protein coding RNA 1
|
|
|
0.670 |
0.500 |
SNORD116-1 |
|
small nucleolar RNA, C/D box 116-1
|
|
|
0.682 |
0.423 |
MKRN3-AS1 |
|
MKRN3 antisense RNA 1
|
|
|
0.682 |
0.423 |
SNORD115-1 |
|
small nucleolar RNA, C/D box 115-1
|
|
|
0.682 |
0.423 |
IPW |
|
imprinted in Prader-Willi syndrome
|
|
|
0.682 |
0.423 |
HYMAI |
|
hydatidiform mole associated and imprinted
|
|
|
0.670 |
0.538 |
SCN1A-AS1 |
|
SCN1A and SCN9A antisense RNA 1
|
|
|
0.636 |
0.346 |
TRNN |
|
tRNA
|
|
|
0.682 |
0.577 |
FRAXA |
|
fragile site, folic acid type, rare, fra(X)(q27.3) A (macroorchidism, mental retardation)
|
|
|
0.641 |
0.462 |
FRAXE |
|
fragile site, folic acid type, rare, fra(X)(q28) E
|
|
|
0.636 |
0.462 |
HOXB@ |
|
homeobox B cluster
|
|
|
0.631 |
0.538 |