Variant report
| Variant |
rs531248075 |
| Chromosome Location |
chr10:44246870-44246871 |
| allele |
A/C
|
| Outlinks |
Ensembl
UCSC
|
Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page:
1
| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
esv3386306 |
chr10:44246727-44247174 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
Chromatin state (count:3 , 50 per page) page:
1
| No. |
Chromosome Location |
Chromatin state |
Cell line |
Tissue |
| 1 |
chr10:44244800-44248600 |
Weak transcription |
iPS DF 19.11 Cell Line |
embryonic stem cell
|
| 2 |
chr10:44246200-44248000 |
Weak transcription |
Fetal Adrenal Gland |
Adrenal Gland
|
| 3 |
chr10:44246600-44248400 |
Weak transcription |
Pancreas |
Pancrea
|
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