Variant report
Variant | rs61860007 |
---|---|
Chromosome Location | chr10:44000382-44000383 |
allele | A/G |
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] |
---|---|
rs10899858 | 1.00[ASN][1000 genomes] |
rs10899859 | 1.00[ASN][1000 genomes] |
rs11238518 | 1.00[ASN][1000 genomes] |
rs11238519 | 1.00[ASN][1000 genomes] |
rs11238520 | 1.00[ASN][1000 genomes] |
rs11238531 | 1.00[ASN][1000 genomes] |
rs11238533 | 1.00[ASN][1000 genomes] |
rs11238547 | 1.00[ASN][1000 genomes] |
rs11238570 | 0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11238591 | 1.00[ASN][1000 genomes] |
rs11238605 | 1.00[ASN][1000 genomes] |
rs11238628 | 1.00[ASN][1000 genomes] |
rs11238635 | 1.00[ASN][1000 genomes] |
rs12263722 | 1.00[ASN][1000 genomes] |
rs12356024 | 1.00[ASN][1000 genomes] |
rs12356570 | 1.00[ASN][1000 genomes] |
rs12358200 | 1.00[ASN][1000 genomes] |
rs12359520 | 1.00[ASN][1000 genomes] |
rs12359825 | 1.00[ASN][1000 genomes] |
rs12359980 | 0.82[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs17154006 | 1.00[ASN][1000 genomes] |
rs17154012 | 1.00[ASN][1000 genomes] |
rs17154020 | 1.00[ASN][1000 genomes] |
rs17366560 | 1.00[ASN][1000 genomes] |
rs17447133 | 1.00[ASN][1000 genomes] |
rs17447468 | 1.00[ASN][1000 genomes] |
rs17447580 | 1.00[ASN][1000 genomes] |
rs34966945 | 1.00[ASN][1000 genomes] |
rs41313824 | 1.00[ASN][1000 genomes] |
rs4646975 | 1.00[ASN][1000 genomes] |
rs4948720 | 1.00[ASN][1000 genomes] |
rs56120769 | 1.00[ASN][1000 genomes] |
rs57740712 | 1.00[ASN][1000 genomes] |
rs59220072 | 1.00[ASN][1000 genomes] |
rs60163354 | 0.91[AFR][1000 genomes];0.89[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs61858993 | 1.00[ASN][1000 genomes] |
rs61858995 | 1.00[ASN][1000 genomes] |
rs61859001 | 1.00[ASN][1000 genomes] |
rs61859177 | 1.00[ASN][1000 genomes] |
rs61859178 | 1.00[ASN][1000 genomes] |
rs61859179 | 1.00[ASN][1000 genomes] |
rs61859180 | 1.00[ASN][1000 genomes] |
rs61859181 | 1.00[ASN][1000 genomes] |
rs61859182 | 1.00[ASN][1000 genomes] |
rs61859185 | 1.00[ASN][1000 genomes] |
rs61859203 | 1.00[ASN][1000 genomes] |
rs61859204 | 1.00[ASN][1000 genomes] |
rs61859207 | 1.00[ASN][1000 genomes] |
rs61859221 | 1.00[ASN][1000 genomes] |
rs61859445 | 1.00[ASN][1000 genomes] |
rs61859998 | 1.00[ASN][1000 genomes] |
rs61860889 | 1.00[ASN][1000 genomes] |
rs67284218 | 1.00[ASN][1000 genomes] |
rs7073767 | 1.00[ASN][1000 genomes] |
rs7079012 | 1.00[ASN][1000 genomes] |
rs7084706 | 1.00[ASN][1000 genomes] |
rs7093434 | 1.00[ASN][1000 genomes] |
rs7100846 | 1.00[ASN][1000 genomes] |
rs7900284 | 1.00[ASN][1000 genomes] |
rs7903467 | 1.00[ASN][1000 genomes] |
rs7905073 | 1.00[ASN][1000 genomes] |
rs7906484 | 1.00[ASN][1000 genomes] |
rs7913352 | 1.00[ASN][1000 genomes] |
rs7916345 | 1.00[ASN][1000 genomes] |
rs7920408 | 1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv895088 | chr10:43871999-44003101 | Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 67 gene(s) | inside rSNPs | diseases |
2 | nsv1046236 | chr10:43968075-44012933 | ZNF genes & repeats Weak transcription Strong transcription Enhancers | Chromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
3 | nsv1051325 | chr10:43988273-44022473 | ZNF genes & repeats Weak transcription Enhancers | TF binding regionChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
4 | esv1797129 | chr10:43996713-44002994 | ZNF genes & repeats Weak transcription Enhancers | n/a | n/a | inside rSNPs | diseases |
5 | esv275081 | chr10:43996713-44018932 | Weak transcription ZNF genes & repeats Enhancers | TF binding regionChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
6 | esv1816330 | chr10:43999354-44002994 | Weak transcription Enhancers ZNF genes & repeats | n/a | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr10:43987400-44003200 | Weak transcription | Duodenum Smooth Muscle | Duodenum |
2 | chr10:43994600-44002200 | Weak transcription | Brain Inferior Temporal Lobe | brain |
3 | chr10:43996400-44002400 | Weak transcription | Brain Cingulate Gyrus | brain |
4 | chr10:43998000-44005000 | Weak transcription | Brain Hippocampus Middle | brain |