Variant report
Variant | rs589427 |
---|---|
Chromosome Location | chr2:31872513-31872514 |
allele | A/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:1 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr2:31871510..31874229-chr2:31876671..31879476,2 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs12467911 | 0.93[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap] |
rs12479192 | 0.80[ASN][1000 genomes] |
rs1510917 | 0.82[ASN][1000 genomes] |
rs2208532 | 0.87[CHB][hapmap];1.00[JPT][hapmap] |
rs2268799 | 0.83[ASN][1000 genomes] |
rs2300697 | 0.87[CHB][hapmap];1.00[JPT][hapmap] |
rs2300699 | 0.80[EUR][1000 genomes] |
rs2300701 | 0.87[CHB][hapmap];1.00[JPT][hapmap] |
rs2754530 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes] |
rs4952197 | 0.82[CHB][hapmap] |
rs4952244 | 0.81[CEU][hapmap];0.85[JPT][hapmap] |
rs499362 | 0.85[ASN][1000 genomes] |
rs502139 | 0.80[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs522638 | 0.87[CHB][hapmap];0.81[JPT][hapmap];0.81[YRI][hapmap];0.83[EUR][1000 genomes] |
rs523349 | 0.88[CEU][hapmap];0.87[CHB][hapmap];0.82[JPT][hapmap];0.95[YRI][hapmap];0.90[EUR][1000 genomes] |
rs524345 | 0.82[AFR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs527112 | 0.87[AFR][1000 genomes];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs539213 | 0.83[AFR][1000 genomes];0.93[ASN][1000 genomes] |
rs553464 | 0.81[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs559555 | 0.85[ASN][1000 genomes] |
rs569320 | 0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs599300 | 0.85[ASN][1000 genomes] |
rs607294 | 0.80[AMR][1000 genomes];0.81[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs608574 | 0.90[ASN][1000 genomes] |
rs623419 | 0.88[ASN][1000 genomes] |
rs632148 | 0.81[CEU][hapmap];0.87[CHB][hapmap];0.90[JPT][hapmap];0.80[YRI][hapmap];0.83[EUR][1000 genomes] |
rs6748639 | 0.81[ASN][1000 genomes] |
rs676033 | 0.82[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.83[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs681482 | 0.93[AMR][1000 genomes];0.85[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs682895 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs765138 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes] |
rs806645 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes] |
Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page:
1
No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv532648 | chr2:31591498-32312698 | Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 39 gene(s) | inside rSNPs | diseases |
2 | nsv1002988 | chr2:31767131-31996924 | Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Genic enhancers Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
3 | esv3376782 | chr2:31861607-32046180 | Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer | TF binding regionChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:31861000-31873600 | Weak transcription | Liver | Liver |