Variant report
Variant | rs41525348 |
---|---|
Chromosome Location | chr1:84269426-84269427 |
allele | G/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
No data |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10489508 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs10493742 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs10493743 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs11163863 | 1.00[ASN][1000 genomes] |
rs11163864 | 1.00[ASN][1000 genomes] |
rs12116464 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs12116522 | 1.00[ASN][1000 genomes] |
rs12116857 | 1.00[ASN][1000 genomes] |
rs12117386 | 1.00[ASN][1000 genomes] |
rs12117716 | 1.00[ASN][1000 genomes] |
rs12118371 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs12118428 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs12119338 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs12119854 | 1.00[ASN][1000 genomes] |
rs12120380 | 1.00[ASN][1000 genomes] |
rs12120801 | 1.00[ASN][1000 genomes] |
rs12120817 | 1.00[ASN][1000 genomes] |
rs12120905 | 1.00[ASN][1000 genomes] |
rs12120992 | 1.00[ASN][1000 genomes] |
rs12121058 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs12121629 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs12121952 | 1.00[ASN][1000 genomes] |
rs12123247 | 1.00[ASN][1000 genomes] |
rs12123323 | 1.00[ASN][1000 genomes] |
rs12125111 | 1.00[ASN][1000 genomes] |
rs12125251 | 1.00[ASN][1000 genomes] |
rs12125932 | 1.00[ASN][1000 genomes] |
rs12126397 | 1.00[ASN][1000 genomes] |
rs12126515 | 1.00[ASN][1000 genomes] |
rs12127196 | 1.00[ASN][1000 genomes] |
rs12127526 | 1.00[ASN][1000 genomes] |
rs12127657 | 1.00[ASN][1000 genomes] |
rs12128942 | 1.00[ASN][1000 genomes] |
rs12129276 | 1.00[ASN][1000 genomes] |
rs12131968 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs12132861 | 1.00[ASN][1000 genomes] |
rs12133196 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs12133949 | 1.00[ASN][1000 genomes] |
rs12135099 | 1.00[ASN][1000 genomes] |
rs12135679 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs12135764 | 1.00[ASN][1000 genomes] |
rs12136835 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs12138207 | 1.00[ASN][1000 genomes] |
rs12138857 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs12139383 | 1.00[ASN][1000 genomes] |
rs12140562 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs12140964 | 1.00[ASN][1000 genomes] |
rs12141004 | 1.00[ASN][1000 genomes] |
rs12141166 | 1.00[ASN][1000 genomes] |
rs12142059 | 1.00[ASN][1000 genomes] |
rs12142944 | 1.00[CHB][hapmap] |
rs12143951 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs12144066 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs12144704 | 1.00[ASN][1000 genomes] |
rs12145472 | 1.00[ASN][1000 genomes] |
rs12145760 | 1.00[ASN][1000 genomes] |
rs1408474 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs1408475 | 1.00[ASN][1000 genomes] |
rs17130437 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs17130475 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs17475494 | 1.00[ASN][1000 genomes] |
rs17534879 | 1.00[ASN][1000 genomes] |
rs1925712 | 1.00[ASN][1000 genomes] |
rs2006 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs2031371 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs2147394 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs2181901 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs2389650 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs41293003 | 1.00[ASN][1000 genomes] |
rs41293005 | 1.00[ASN][1000 genomes] |
rs41423448 | 1.00[ASN][1000 genomes] |
rs4258240 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs4282844 | 1.00[ASN][1000 genomes] |
rs4387198 | 1.00[ASN][1000 genomes] |
rs4437897 | 1.00[ASN][1000 genomes] |
rs45515591 | 1.00[ASN][1000 genomes] |
rs56159052 | 1.00[ASN][1000 genomes] |
rs58842909 | 1.00[ASN][1000 genomes] |
rs61483809 | 1.00[ASN][1000 genomes] |
rs6576912 | 1.00[ASN][1000 genomes] |
rs6576913 | 1.00[ASN][1000 genomes] |
rs6576916 | 1.00[ASN][1000 genomes] |
rs6678773 | 1.00[ASN][1000 genomes] |
rs6690381 | 1.00[ASN][1000 genomes] |
rs6700983 | 1.00[ASN][1000 genomes] |
rs74096420 | 1.00[ASN][1000 genomes] |
rs74096423 | 1.00[ASN][1000 genomes] |
rs7519127 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs9645391 | 1.00[ASN][1000 genomes] |
rs9645396 | 1.00[ASN][1000 genomes] |
rs9645397 | 1.00[ASN][1000 genomes] |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:84265800-84270400 | Weak transcription | Pancreas | Pancrea |
2 | chr1:84268400-84270400 | Weak transcription | Cortex derived primary cultured neurospheres | brain |
3 | chr1:84268800-84270200 | Weak transcription | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
4 | chr1:84268800-84270200 | Weak transcription | H9 Derived Neuron Cultured Cells | ES cell derived |
5 | chr1:84268800-84270400 | Weak transcription | Aorta | Aorta |
6 | chr1:84268800-84273400 | Weak transcription | Adipose Nuclei | Adipose |
7 | chr1:84268800-84273600 | Weak transcription | Liver | Liver |
8 | chr1:84269400-84270200 | Weak transcription | Pancreatic Islets | Pancreatic Islet |