Variant report
| Variant |
rs4948799 |
| Chromosome Location |
chr10:44469683-44469684 |
| allele |
C/G
|
| Outlinks |
Ensembl
UCSC
|
rSNPs within LD-proxies of this variant (count:3)
Chromatin state (count:10 , 50 per page) page:
1
| No. |
Chromosome Location |
Chromatin state |
Cell line |
Tissue |
| 1 |
chr10:44462000-44474400 |
Weak transcription |
Left Ventricle |
heart
|
| 2 |
chr10:44462400-44475200 |
Weak transcription |
Right Atrium |
heart
|
| 3 |
chr10:44466400-44476000 |
Weak transcription |
Right Ventricle |
heart
|
| 4 |
chr10:44467000-44473000 |
Weak transcription |
Spleen |
Spleen
|
| 5 |
chr10:44468400-44470200 |
Enhancers |
Fetal Muscle Leg |
muscle
|
| 6 |
chr10:44468600-44469800 |
Enhancers |
Fetal Muscle Trunk |
muscle
|
| 7 |
chr10:44468800-44470000 |
Enhancers |
Skeletal Muscle Male |
skeletal muscle
|
| 8 |
chr10:44469000-44470200 |
Enhancers |
Fetal Intestine Small |
intestine
|
| 9 |
chr10:44469000-44471600 |
Enhancers |
Adipose Nuclei |
Adipose
|
| 10 |
chr10:44469600-44469800 |
Enhancers |
Gastric |
stomach
|
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