Variant report
Variant | rs72655020 |
---|---|
Chromosome Location | chr8:63785488-63785489 |
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] |
---|---|
rs11988327 | 1.00[ASN][1000 genomes] |
rs11995803 | 1.00[ASN][1000 genomes] |
rs72655003 | 1.00[ASN][1000 genomes] |
rs72655011 | 0.91[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72655031 | 0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72655032 | 0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72655033 | 0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72655040 | 0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72655052 | 0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72655076 | 0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72656520 | 1.00[ASN][1000 genomes] |
rs72656523 | 1.00[ASN][1000 genomes] |
rs72656530 | 1.00[ASN][1000 genomes] |
rs72656539 | 1.00[ASN][1000 genomes] |
rs72656545 | 1.00[ASN][1000 genomes] |
rs72656600 | 1.00[ASN][1000 genomes] |
rs72658335 | 1.00[ASN][1000 genomes] |
rs72658345 | 1.00[ASN][1000 genomes] |
rs72658355 | 1.00[ASN][1000 genomes] |
rs72658358 | 1.00[ASN][1000 genomes] |
rs72658363 | 1.00[ASN][1000 genomes] |
rs72658377 | 1.00[ASN][1000 genomes] |
rs72658378 | 1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1018879 | chr8:63281724-63937632 | Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
2 | nsv831341 | chr8:63658694-63852213 | Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
3 | nsv1033527 | chr8:63673915-64073735 | Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 18 gene(s) | inside rSNPs | diseases |
4 | nsv890962 | chr8:63708519-63812686 | Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:63782000-63792200 | Weak transcription | Cortex derived primary cultured neurospheres | brain |