Variant report
Variant | rs7585325 |
---|---|
Chromosome Location | chr2:142278425-142278426 |
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] |
---|---|
rs10165979 | 1.00[AMR][1000 genomes] |
rs10176397 | 1.00[AMR][1000 genomes] |
rs10176693 | 1.00[AMR][1000 genomes] |
rs10187180 | 1.00[AMR][1000 genomes] |
rs10200578 | 1.00[AMR][1000 genomes] |
rs10200782 | 0.81[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs10200845 | 1.00[AMR][1000 genomes] |
rs11887261 | 1.00[AMR][1000 genomes] |
rs11904458 | 1.00[AMR][1000 genomes] |
rs12466189 | 1.00[AMR][1000 genomes] |
rs12472734 | 1.00[AMR][1000 genomes] |
rs12617980 | 1.00[AMR][1000 genomes] |
rs12618575 | 1.00[AMR][1000 genomes] |
rs12691613 | 1.00[AMR][1000 genomes] |
rs12691614 | 0.90[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs12691615 | 1.00[AMR][1000 genomes] |
rs1483138 | 1.00[AMR][1000 genomes] |
rs1483152 | 1.00[AMR][1000 genomes] |
rs2054655 | 0.81[AFR][1000 genomes] |
rs2128694 | 1.00[AMR][1000 genomes] |
rs2170667 | 0.90[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs2381110 | 1.00[AMR][1000 genomes] |
rs2381111 | 1.00[AMR][1000 genomes] |
rs2381112 | 1.00[AMR][1000 genomes] |
rs2381113 | 1.00[AMR][1000 genomes] |
rs2381192 | 1.00[AMR][1000 genomes] |
rs3935992 | 1.00[AMR][1000 genomes] |
rs4008531 | 1.00[AMR][1000 genomes] |
rs4245859 | 1.00[AMR][1000 genomes] |
rs4264515 | 1.00[AMR][1000 genomes] |
rs4296372 | 1.00[AMR][1000 genomes] |
rs4366842 | 1.00[AMR][1000 genomes] |
rs4396652 | 1.00[AMR][1000 genomes] |
rs4439901 | 1.00[AMR][1000 genomes] |
rs4441406 | 1.00[AMR][1000 genomes] |
rs4476294 | 1.00[AMR][1000 genomes] |
rs4477847 | 1.00[AMR][1000 genomes] |
rs4555282 | 1.00[AMR][1000 genomes] |
rs4954909 | 1.00[AMR][1000 genomes] |
rs4954913 | 1.00[AMR][1000 genomes] |
rs6429896 | 1.00[AMR][1000 genomes] |
rs6429901 | 1.00[AMR][1000 genomes] |
rs6429902 | 1.00[AMR][1000 genomes] |
rs6706356 | 1.00[AMR][1000 genomes] |
rs6706377 | 1.00[AMR][1000 genomes] |
rs6707441 | 1.00[AMR][1000 genomes] |
rs6708438 | 1.00[AMR][1000 genomes] |
rs6710020 | 1.00[AMR][1000 genomes] |
rs6713043 | 1.00[AMR][1000 genomes] |
rs6718844 | 1.00[AMR][1000 genomes] |
rs6737585 | 1.00[AMR][1000 genomes] |
rs6749472 | 1.00[AMR][1000 genomes] |
rs7557631 | 1.00[AMR][1000 genomes] |
rs7572480 | 1.00[AMR][1000 genomes] |
rs7582623 | 1.00[AMR][1000 genomes] |
rs7593866 | 1.00[AMR][1000 genomes] |
rs7607376 | 0.90[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs983197 | 1.00[AMR][1000 genomes] |
rs983198 | 1.00[AMR][1000 genomes] |
rs983199 | 1.00[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv817518 | chr2:141714174-142287302 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
2 | nsv583203 | chr2:142055133-142378975 | Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers | Chromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
3 | nsv875240 | chr2:142199421-142347455 | Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer | Chromatin interactive region | 2 gene(s) | inside rSNPs | n/a |
4 | nsv470491 | chr2:142254119-142299923 | Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer | Chromatin interactive region | 2 gene(s) | inside rSNPs | n/a |
5 | nsv834393 | chr2:142256714-142431564 | Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | n/a |
6 | nsv583210 | chr2:142259592-142295042 | Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer | Chromatin interactive region | 2 gene(s) | inside rSNPs | n/a |
7 | nsv459629 | chr2:142263400-142295042 | Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer | Chromatin interactive region | 2 gene(s) | inside rSNPs | n/a |
8 | nsv583211 | chr2:142263400-142295042 | Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer | Chromatin interactive region | 2 gene(s) | inside rSNPs | n/a |
9 | nsv583212 | chr2:142263979-142309330 | Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer | Chromatin interactive region | 2 gene(s) | inside rSNPs | n/a |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:142277200-142279000 | Enhancers | Brain Angular Gyrus | brain |
2 | chr2:142277200-142279000 | Enhancers | Brain Inferior Temporal Lobe | brain |
3 | chr2:142277800-142278600 | Enhancers | Ganglion Eminence derived primary cultured neurospheres | brain |
4 | chr2:142278200-142278600 | Active TSS | Brain Anterior Caudate | brain |
5 | chr2:142278200-142279600 | Weak transcription | Brain Cingulate Gyrus | brain |
6 | chr2:142278200-142280600 | Enhancers | Brain Substantia Nigra | brain |
7 | chr2:142278400-142278600 | Active TSS | Brain Hippocampus Middle | brain |