Variant report
Variant | rs975588 |
---|---|
Chromosome Location | chr4:173323412-173323413 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
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(count:2 , 50 per page) page:
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rs_ID | r2[population] |
---|---|
rs11132935 | 0.95[JPT][hapmap] |
rs1160452 | 1.00[ASW][hapmap];0.89[CEU][hapmap];0.95[GIH][hapmap];1.00[LWK][hapmap];0.86[MEX][hapmap];0.89[TSI][hapmap] |
rs11726268 | 0.90[ASN][1000 genomes] |
rs12502211 | 0.95[JPT][hapmap] |
rs12509779 | 0.95[JPT][hapmap] |
rs12511688 | 0.80[CEU][hapmap];0.85[JPT][hapmap];0.84[AFR][1000 genomes] |
rs13101363 | 0.85[CHB][hapmap];0.93[CHD][hapmap];0.95[JPT][hapmap] |
rs13434538 | 0.85[CHB][hapmap];0.95[JPT][hapmap];0.91[ASN][1000 genomes] |
rs1484019 | 0.93[CHD][hapmap];0.95[JPT][hapmap] |
rs1496711 | 0.81[CEU][hapmap];0.87[GIH][hapmap];1.00[LWK][hapmap];0.82[MEX][hapmap] |
rs1552247 | 0.90[JPT][hapmap] |
rs167991 | 0.85[CHB][hapmap];0.95[JPT][hapmap];0.91[ASN][1000 genomes] |
rs17288825 | 0.95[JPT][hapmap] |
rs17288971 | 0.95[JPT][hapmap] |
rs17289279 | 0.90[JPT][hapmap] |
rs17305821 | 1.00[LWK][hapmap] |
rs2047341 | 0.81[CEU][hapmap];1.00[LWK][hapmap] |
rs2332481 | 0.84[CHB][hapmap];0.86[JPT][hapmap];0.91[ASN][1000 genomes] |
rs2626608 | 0.85[CHD][hapmap];0.81[JPT][hapmap] |
rs2930204 | 0.91[JPT][hapmap] |
rs333398 | 0.91[ASN][1000 genomes] |
rs333399 | 0.91[ASN][1000 genomes] |
rs333408 | 0.90[ASN][1000 genomes] |
rs34069532 | 0.95[ASN][1000 genomes] |
rs4140 | 1.00[LWK][hapmap] |
rs4692917 | 0.85[CHB][hapmap];0.93[CHD][hapmap];0.95[JPT][hapmap];0.91[ASN][1000 genomes] |
rs6553625 | 0.91[JPT][hapmap] |
rs6834066 | 0.89[CEU][hapmap] |
rs6836161 | 0.93[ASN][1000 genomes] |
rs768425 | 0.85[CHB][hapmap];0.93[CHD][hapmap];0.95[JPT][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1031592 | chr4:173112542-173662991 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
2 | nsv537359 | chr4:173112542-173662991 | Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
3 | nsv534293 | chr4:173121379-173606082 | Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
4 | nsv880416 | chr4:173287422-173388217 | Enhancers Weak transcription ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
5 | nsv1031327 | chr4:173306405-173465248 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
No data |