Variant report
| Variant |
rs182797915 |
| Chromosome Location |
chr3:50766914-50766915 |
| allele |
C/G
|
| 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 |
nsv237212 |
chr3:50766440-50767231 |
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 |
chr3:50763800-50772800 |
Weak transcription |
iPS DF 19.11 Cell Line |
embryonic stem cell
|
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