Variant report
| Variant |
rs58651667 |
| Chromosome Location |
chr2:184276691-184276692 |
| allele |
A/G
|
| Outlinks |
Ensembl
UCSC
|
rSNPs within LD-proxies of this variant (count:1)
| rs_ID |
r2[population] |
| rs73980603 |
1.00[EUR][1000 genomes] |
Chromatin state (count:5 , 50 per page) page:
1
| No. |
Chromosome Location |
Chromatin state |
Cell line |
Tissue |
| 1 |
chr2:184274200-184281600 |
Weak transcription |
H9 Cell Line |
embryonic stem cell
|
| 2 |
chr2:184275600-184281400 |
Weak transcription |
iPS-20b Cell Line |
embryonic stem cell
|
| 3 |
chr2:184275800-184281400 |
Weak transcription |
H1 Cell Line |
embryonic stem cell
|
| 4 |
chr2:184275800-184281400 |
Weak transcription |
iPS DF 6.9 Cell Line |
embryonic stem cell
|
| 5 |
chr2:184276000-184281600 |
Weak transcription |
ES-I3 Cell Line |
embryonic stem cell
|
Quick Search:
Input of quick search could be:
what's new
Quick links
