Variant report
Variant | rs4945618 |
---|---|
Chromosome Location | chr6:118558351-118558352 |
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] |
---|---|
rs11153725 | 0.81[CHB][hapmap];0.83[JPT][hapmap];0.85[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs12202829 | 0.83[AMR][1000 genomes] |
rs17079862 | 1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs176014 | 0.91[CEU][hapmap];0.90[CHB][hapmap];0.90[EUR][1000 genomes] |
rs1874082 | 0.82[EUR][1000 genomes] |
rs190756 | 0.95[CHB][hapmap] |
rs1923282 | 0.91[CEU][hapmap];0.94[CHB][hapmap] |
rs205915 | 0.83[AMR][1000 genomes] |
rs205916 | 0.83[AMR][1000 genomes] |
rs2105020 | 0.83[AMR][1000 genomes] |
rs2356077 | 0.83[AMR][1000 genomes] |
rs281866 | 0.96[CEU][hapmap];0.95[CHB][hapmap];0.84[JPT][hapmap];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs281869 | 0.95[CEU][hapmap];0.95[CHB][hapmap];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs281872 | 0.91[CEU][hapmap];0.95[CHB][hapmap];0.84[JPT][hapmap];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs283067 | 0.81[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs283083 | 0.91[CEU][hapmap];0.90[CHB][hapmap];0.84[EUR][1000 genomes] |
rs2883849 | 0.95[CEU][hapmap];0.95[CHB][hapmap];0.84[JPT][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs387266 | 0.81[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs413876 | 0.95[CEU][hapmap];0.95[CHB][hapmap];0.83[EUR][1000 genomes] |
rs427027 | 0.91[CEU][hapmap];0.84[CHB][hapmap];0.84[EUR][1000 genomes] |
rs450093 | 1.00[CEU][hapmap];0.95[CHB][hapmap];0.89[EUR][1000 genomes] |
rs7762823 | 0.81[CHB][hapmap] |
rs9320646 | 0.95[CEU][hapmap];0.95[CHB][hapmap];0.89[JPT][hapmap];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs9385038 | 0.95[CEU][hapmap];0.95[CHB][hapmap];0.89[JPT][hapmap];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs9387565 | 0.83[AMR][1000 genomes] |
rs9398485 | 0.83[AMR][1000 genomes] |
rs9489326 | 0.81[CHB][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv530526 | chr6:118027339-118718476 | Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive region | 4 gene(s) | inside rSNPs | diseases |
2 | nsv428153 | chr6:118430517-118586974 | Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
3 | nsv1030089 | chr6:118436482-118604516 | Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
4 | nsv538427 | chr6:118436482-118604516 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
5 | nsv532051 | chr6:118551027-119044197 | Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 9 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:118546400-118564000 | Weak transcription | Ganglion Eminence derived primary cultured neurospheres | brain |
2 | chr6:118553400-118564200 | Weak transcription | Fetal Brain Female | brain |
3 | chr6:118557800-118558800 | Strong transcription | Cortex derived primary cultured neurospheres | brain |