Variant report
| Variant |
rs562112990 |
| Chromosome Location |
chr18:45095543-45095544 |
| allele |
A/C
|
| 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 |
esv3316804 |
chr18:45095098-45096190 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 2 |
esv3316803 |
chr18:45095150-45096162 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 3 |
esv3316802 |
chr18:45095184-45096134 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 4 |
esv3316805 |
chr18:45095272-45096071 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 5 |
esv15393 |
chr18:45095294-45096085 |
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
|
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