Variant report
| Variant |
rs11572468 |
| Chromosome Location |
chr1:217126800-217126801 |
| allele |
A/G
|
| Outlinks |
Ensembl
UCSC
|
rSNPs within LD-proxies of this variant (count:8)
Chromatin state (count:9 , 50 per page) page:
1
| No. |
Chromosome Location |
Chromatin state |
Cell line |
Tissue |
| 1 |
chr1:217122400-217146200 |
Weak transcription |
Pancreas |
Pancrea
|
| 2 |
chr1:217125200-217135400 |
Weak transcription |
Fetal Heart |
heart
|
| 3 |
chr1:217125400-217127000 |
Enhancers |
HUES48 Cell Line |
embryonic stem cell
|
| 4 |
chr1:217125600-217127000 |
Enhancers |
iPS-15b Cell Line |
embryonic stem cell
|
| 5 |
chr1:217125800-217126800 |
Weak transcription |
Left Ventricle |
heart
|
| 6 |
chr1:217126000-217126800 |
Enhancers |
H9 Cell Line |
embryonic stem cell
|
| 7 |
chr1:217126000-217127000 |
Enhancers |
HUES64 Cell Line |
embryonic stem cell
|
| 8 |
chr1:217126200-217127000 |
Enhancers |
iPS DF 19.11 Cell Line |
embryonic stem cell
|
| 9 |
chr1:217126800-217127000 |
Enhancers |
Left Ventricle |
heart
|
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