Variant report
Variant | rs4848246 |
---|---|
Chromosome Location | chr2:125315822-125315823 |
allele | A/G |
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] |
---|---|
rs10185849 | 0.91[CHB][hapmap] |
rs10188201 | 0.91[CHB][hapmap];0.87[JPT][hapmap] |
rs10496637 | 0.91[CHB][hapmap] |
rs11123050 | 0.81[CHB][hapmap] |
rs11682973 | 0.90[CHB][hapmap];0.90[JPT][hapmap] |
rs11888767 | 0.82[CHB][hapmap] |
rs11896097 | 0.82[CHB][hapmap] |
rs11899391 | 0.80[CHB][hapmap] |
rs12464032 | 0.82[CHB][hapmap] |
rs12464048 | 0.82[CHB][hapmap] |
rs12468237 | 0.82[CHB][hapmap] |
rs12470517 | 0.82[CHB][hapmap] |
rs12623983 | 0.91[CHB][hapmap] |
rs12711680 | 0.84[CEU][hapmap];0.90[CHB][hapmap] |
rs12995531 | 0.80[CHB][hapmap] |
rs13030176 | 0.82[CHB][hapmap] |
rs1504006 | 0.82[CHB][hapmap] |
rs1504008 | 0.82[CHB][hapmap] |
rs1504009 | 0.82[CHB][hapmap] |
rs17011693 | 0.91[CHB][hapmap];0.81[JPT][hapmap];0.80[ASN][1000 genomes] |
rs17011723 | 0.82[CHB][hapmap] |
rs17011727 | 0.83[CHB][hapmap] |
rs17011734 | 0.82[CHB][hapmap] |
rs1857690 | 0.81[CHB][hapmap] |
rs1857691 | 0.82[CHB][hapmap] |
rs1857694 | 0.82[CHB][hapmap] |
rs1910527 | 0.91[CHB][hapmap] |
rs2047875 | 0.86[CHB][hapmap];0.81[JPT][hapmap] |
rs2047876 | 0.91[CHB][hapmap] |
rs2047877 | 0.91[CHB][hapmap];0.87[JPT][hapmap];0.81[ASN][1000 genomes] |
rs4402762 | 0.81[CHB][hapmap] |
rs6541959 | 0.91[CHB][hapmap];0.87[JPT][hapmap] |
rs6707944 | 0.91[CHB][hapmap];0.87[JPT][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1014610 | chr2:125124983-125350342 | Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
2 | nsv834357 | chr2:125258157-125421507 | Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
3 | esv3437542 | chr2:125314184-125315932 | Enhancers | n/a | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:125315800-125316600 | Enhancers | hESC Derived CD56+ Ectoderm Cultured Cells | ES cell derived |
2 | chr2:125315800-125317000 | Enhancers | Fetal Brain Male | brain |