Variant report
Variant | rs35550109 |
---|---|
Chromosome Location | chr4:62462234-62462235 |
allele | C/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] |
---|---|
rs10004368 | 0.86[JPT][hapmap];0.91[MEX][hapmap] |
rs10007185 | 0.82[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs10018746 | 0.82[ASW][hapmap];0.86[CEU][hapmap];0.81[MKK][hapmap];0.94[TSI][hapmap];0.86[YRI][hapmap] |
rs10023817 | 0.84[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs10866123 | 0.95[EUR][1000 genomes] |
rs11131331 | 0.88[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs11131333 | 0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs11131337 | 0.85[JPT][hapmap] |
rs11131340 | 0.91[JPT][hapmap] |
rs11931258 | 0.91[JPT][hapmap] |
rs11941524 | 0.92[EUR][1000 genomes] |
rs12233859 | 0.81[JPT][hapmap] |
rs12507326 | 0.81[JPT][hapmap] |
rs12642037 | 0.91[JPT][hapmap];0.83[MEX][hapmap] |
rs12642315 | 0.84[CEU][hapmap];0.89[JPT][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs12715703 | 0.85[EUR][1000 genomes] |
rs1497897 | 0.81[JPT][hapmap] |
rs1542834 | 0.81[JPT][hapmap] |
rs1846161 | 1.00[JPT][hapmap];0.81[AFR][1000 genomes];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs1948616 | 0.87[MEX][hapmap] |
rs2036199 | 0.91[JPT][hapmap] |
rs2172802 | 0.82[ASW][hapmap];0.95[CEU][hapmap];0.90[GIH][hapmap];0.83[MKK][hapmap];1.00[TSI][hapmap];0.93[YRI][hapmap];0.95[EUR][1000 genomes] |
rs4860422 | 0.81[JPT][hapmap] |
rs6551636 | 0.86[JPT][hapmap] |
rs7675385 | 0.89[JPT][hapmap] |
rs7690118 | 0.85[JPT][hapmap] |
rs7690595 | 0.88[EUR][1000 genomes] |
rs9991244 | 0.85[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv868844 | chr4:62241702-62497248 | Weak transcription Enhancers Bivalent/Poised TSS Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
2 | nsv461377 | chr4:62368762-62883431 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
3 | nsv594328 | chr4:62368762-62883431 | Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
4 | nsv1004815 | chr4:62398737-62553769 | ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
5 | nsv537110 | chr4:62398737-62553769 | ZNF genes & repeats Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
6 | nsv594329 | chr4:62416593-62478230 | Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
7 | nsv879077 | chr4:62419426-62545435 | Enhancers ZNF genes & repeats Weak transcription Active TSS Strong transcription Flanking Active TSS | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr4:62451200-62465000 | Weak transcription | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
2 | chr4:62460400-62473400 | Weak transcription | Fetal Adrenal Gland | Adrenal Gland |
3 | chr4:62461200-62478000 | Weak transcription | H9 Derived Neuron Cultured Cells | ES cell derived |
4 | chr4:62461600-62473600 | Weak transcription | Fetal Stomach | stomach |