Variant report
Variant | rs66495951 |
---|---|
Chromosome Location | chr7:78370744-78370745 |
allele | A/C |
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] |
---|---|
rs10229438 | 0.92[EUR][1000 genomes] |
rs10229458 | 0.92[EUR][1000 genomes] |
rs10230190 | 0.92[EUR][1000 genomes] |
rs10230478 | 0.92[EUR][1000 genomes] |
rs10230501 | 0.92[EUR][1000 genomes] |
rs10233033 | 0.92[EUR][1000 genomes] |
rs10243772 | 0.92[EUR][1000 genomes] |
rs10243883 | 0.92[EUR][1000 genomes] |
rs10256389 | 0.89[EUR][1000 genomes] |
rs10273632 | 0.92[EUR][1000 genomes] |
rs10953681 | 0.92[EUR][1000 genomes] |
rs10953687 | 0.92[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs11487098 | 0.93[AFR][1000 genomes] |
rs11760430 | 0.81[EUR][1000 genomes] |
rs11763541 | 0.81[EUR][1000 genomes] |
rs11768142 | 0.89[EUR][1000 genomes] |
rs11768372 | 0.92[EUR][1000 genomes] |
rs11768397 | 0.92[EUR][1000 genomes] |
rs11770561 | 0.81[EUR][1000 genomes] |
rs11770565 | 0.81[EUR][1000 genomes] |
rs11772790 | 0.92[EUR][1000 genomes] |
rs11773249 | 0.94[EUR][1000 genomes] |
rs12113058 | 0.83[ASN][1000 genomes] |
rs12530747 | 0.81[EUR][1000 genomes] |
rs12530771 | 0.81[EUR][1000 genomes] |
rs12530773 | 0.90[EUR][1000 genomes] |
rs12530792 | 0.94[EUR][1000 genomes] |
rs12531353 | 0.94[EUR][1000 genomes] |
rs12531547 | 0.81[EUR][1000 genomes] |
rs12531558 | 0.81[EUR][1000 genomes] |
rs12533182 | 0.94[EUR][1000 genomes] |
rs12533194 | 0.81[EUR][1000 genomes] |
rs12533269 | 0.81[EUR][1000 genomes] |
rs12533873 | 0.81[EUR][1000 genomes] |
rs12534669 | 0.92[EUR][1000 genomes] |
rs12534800 | 0.90[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs12535118 | 0.87[EUR][1000 genomes] |
rs12536030 | 0.83[ASN][1000 genomes] |
rs12536628 | 0.89[EUR][1000 genomes] |
rs12536952 | 0.81[EUR][1000 genomes] |
rs12536959 | 0.81[EUR][1000 genomes] |
rs12536979 | 0.83[ASN][1000 genomes] |
rs12537842 | 0.94[EUR][1000 genomes] |
rs12538687 | 0.81[EUR][1000 genomes] |
rs12538706 | 0.81[EUR][1000 genomes] |
rs12539657 | 0.94[EUR][1000 genomes] |
rs12540478 | 0.81[EUR][1000 genomes] |
rs12540572 | 0.94[EUR][1000 genomes] |
rs12540597 | 0.81[EUR][1000 genomes] |
rs13240011 | 0.89[EUR][1000 genomes] |
rs28502814 | 0.87[EUR][1000 genomes] |
rs28565439 | 0.90[EUR][1000 genomes] |
rs28650857 | 0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs35895217 | 0.89[EUR][1000 genomes] |
rs55669940 | 0.96[EUR][1000 genomes] |
rs55827541 | 0.96[EUR][1000 genomes] |
rs55984124 | 0.89[EUR][1000 genomes] |
rs56161537 | 0.96[EUR][1000 genomes] |
rs56165236 | 0.81[EUR][1000 genomes] |
rs56277847 | 0.89[EUR][1000 genomes] |
rs6946747 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs6953739 | 0.92[EUR][1000 genomes] |
rs727538 | 0.94[AFR][1000 genomes] |
rs73135509 | 0.92[EUR][1000 genomes] |
rs73135518 | 0.92[EUR][1000 genomes] |
rs73135526 | 0.92[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs73135549 | 0.83[ASN][1000 genomes] |
rs73135595 | 0.83[ASN][1000 genomes] |
rs73137205 | 0.83[ASN][1000 genomes] |
rs73137211 | 0.83[ASN][1000 genomes] |
rs73147023 | 0.81[EUR][1000 genomes] |
rs73147031 | 0.81[EUR][1000 genomes] |
rs73147034 | 0.81[EUR][1000 genomes] |
rs73147035 | 0.81[EUR][1000 genomes] |
rs73147039 | 0.81[EUR][1000 genomes] |
rs73147058 | 0.81[EUR][1000 genomes] |
rs73149076 | 0.81[EUR][1000 genomes] |
rs73149082 | 0.81[EUR][1000 genomes] |
rs73149083 | 0.81[EUR][1000 genomes] |
rs73149085 | 0.81[EUR][1000 genomes] |
rs73149086 | 0.81[EUR][1000 genomes] |
rs73149096 | 0.89[EUR][1000 genomes] |
rs73150705 | 0.89[EUR][1000 genomes] |
rs73150708 | 0.89[EUR][1000 genomes] |
rs73150717 | 0.89[EUR][1000 genomes] |
rs73150732 | 0.89[EUR][1000 genomes] |
rs73150760 | 0.90[EUR][1000 genomes] |
rs73150764 | 0.94[EUR][1000 genomes] |
rs73150767 | 0.94[EUR][1000 genomes] |
rs73150783 | 0.94[EUR][1000 genomes] |
rs73150785 | 0.94[EUR][1000 genomes] |
rs73150787 | 0.94[EUR][1000 genomes] |
rs73150791 | 0.94[EUR][1000 genomes] |
rs73150794 | 0.92[EUR][1000 genomes] |
rs73152411 | 0.94[EUR][1000 genomes] |
rs73152421 | 0.94[EUR][1000 genomes] |
rs73152427 | 0.94[EUR][1000 genomes] |
rs73152434 | 0.94[EUR][1000 genomes] |
rs73152443 | 0.94[EUR][1000 genomes] |
rs73152448 | 0.96[EUR][1000 genomes] |
rs73365859 | 0.98[AFR][1000 genomes] |
rs73365861 | 0.93[AFR][1000 genomes] |
rs73365868 | 0.87[AFR][1000 genomes] |
rs73365873 | 0.83[ASN][1000 genomes] |
rs9969173 | 0.98[AFR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1022199 | chr7:78054639-78469370 | Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
2 | nsv538986 | chr7:78054639-78469370 | Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
3 | nsv1019355 | chr7:78319575-78399845 | Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
4 | nsv607657 | chr7:78329795-78483211 | Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
5 | esv1636668 | chr7:78370732-78370744 | Weak transcription Enhancers | n/a | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr7:78361600-78372000 | Weak transcription | Aorta | Aorta |
2 | chr7:78362800-78372200 | Weak transcription | iPS-15b Cell Line | embryonic stem cell |
3 | chr7:78363600-78380400 | Weak transcription | Pancreatic Islets | Pancreatic Islet |
4 | chr7:78364200-78372000 | Weak transcription | iPS DF 6.9 Cell Line | embryonic stem cell |
5 | chr7:78366200-78372000 | Weak transcription | Brain Inferior Temporal Lobe | brain |
6 | chr7:78368000-78375600 | Weak transcription | H1 Cell Line | embryonic stem cell |
7 | chr7:78368200-78372000 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
8 | chr7:78368600-78374400 | Weak transcription | HUES64 Cell Line | embryonic stem cell |
9 | chr7:78368800-78372200 | Weak transcription | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |
10 | chr7:78370600-78371000 | Enhancers | Fetal Brain Male | brain |