Variant report
| Variant |
rs12720779 |
| Chromosome Location |
chr2:21246137-21246138 |
| allele |
A/T
|
| Outlinks |
Ensembl
UCSC
|
rSNPs within LD-proxies of this variant (count:3)
Chromatin state (count:9 , 50 per page) page:
1
| No. |
Chromosome Location |
Chromatin state |
Cell line |
Tissue |
| 1 |
chr2:21234800-21262200 |
Weak transcription |
Ovary |
ovary
|
| 2 |
chr2:21235000-21246600 |
Strong transcription |
Duodenum Mucosa |
Duodenum
|
| 3 |
chr2:21235000-21261800 |
Strong transcription |
Fetal Intestine Large |
intestine
|
| 4 |
chr2:21238400-21246200 |
Strong transcription |
Fetal Intestine Small |
intestine
|
| 5 |
chr2:21240000-21246600 |
Genic enhancers |
HepG2 |
liver
|
| 6 |
chr2:21240600-21250600 |
Weak transcription |
Adipose Nuclei |
Adipose
|
| 7 |
chr2:21242800-21251000 |
Weak transcription |
Left Ventricle |
heart
|
| 8 |
chr2:21245600-21246200 |
Strong transcription |
Aorta |
Aorta
|
| 9 |
chr2:21245600-21246200 |
Genic enhancers |
Liver |
Liver
|
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