Variant report
Variant | rs9327153 |
---|---|
Chromosome Location | chr5:119931774-119931775 |
allele | A/G |
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:
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No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr5:119926337..119929229-chr5:119929732..119932370,2 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10053278 | 0.82[JPT][hapmap] |
rs1037569 | 1.00[CHB][hapmap];0.98[ASN][1000 genomes] |
rs1037570 | 0.96[ASN][1000 genomes] |
rs13173880 | 0.98[ASN][1000 genomes] |
rs1524563 | 0.82[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17500705 | 0.82[JPT][hapmap] |
rs2168216 | 1.00[ASN][1000 genomes] |
rs56126743 | 0.92[ASN][1000 genomes] |
rs6862435 | 0.82[CHB][hapmap] |
rs72792297 | 0.83[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs72792301 | 0.94[ASN][1000 genomes] |
rs7737318 | 0.82[CHB][hapmap];1.00[JPT][hapmap] |
rs9285891 | 0.82[JPT][hapmap] |
rs9285892 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9327154 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9327155 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9327156 | 0.81[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs9327157 | 0.80[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs9686370 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs9716009 | 0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9717178 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs9764195 | 0.90[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs985263 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv532200 | chr5:119317901-120102513 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
2 | nsv830463 | chr5:119806643-119968825 | Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
3 | nsv1031453 | chr5:119843593-120393038 | Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
4 | nsv948613 | chr5:119861955-119999008 | Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
5 | nsv599602 | chr5:119866504-120023393 | Weak transcription Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
6 | nsv949499 | chr5:119869763-119999008 | Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Genic enhancers ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr5:119905600-119934600 | Weak transcription | Muscle Satellite Cultured Cells | -- |
2 | chr5:119907800-119934800 | Weak transcription | HSMM | muscle |
3 | chr5:119931200-119931800 | Enhancers | Osteobl | bone |