Variant report
| Variant |
rs190711020 |
| Chromosome Location |
chr18:45094994-45094995 |
| allele |
A/G
|
| Outlinks |
Ensembl
UCSC
|
Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page:
1
| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
esv3316797 |
chr18:45094836-45095246 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 2 |
esv3316800 |
chr18:45094890-45095222 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 3 |
esv3316798 |
chr18:45094912-45095179 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 4 |
esv3316799 |
chr18:45094961-45095155 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 5 |
esv3316801 |
chr18:45094975-45095155 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
Chromatin state (count:1 , 50 per page) page:
1
| No. |
Chromosome Location |
Chromatin state |
Cell line |
Tissue |
| 1 |
chr18:45090200-45103000 |
Weak transcription |
iPS DF 19.11 Cell Line |
embryonic stem cell
|
Quick Search:
Input of quick search could be:
what's new
Quick links
