Variant report
Variant | rs73283041 |
---|---|
Chromosome Location | chr12:45309771-45309772 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:8)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
(count:8 , 50 per page) page:
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Variant related genes | Relation type |
---|---|
NELL2 | TF binding region |
rs_ID | r2[population] |
---|---|
rs2703058 | 1.00[AMR][1000 genomes] |
rs2710422 | 1.00[AMR][1000 genomes] |
rs2710423 | 1.00[AMR][1000 genomes] |
rs369442 | 1.00[AMR][1000 genomes] |
rs60628417 | 1.00[AMR][1000 genomes] |
rs73277302 | 1.00[AMR][1000 genomes] |
rs73279103 | 1.00[AMR][1000 genomes] |
rs73279110 | 1.00[AMR][1000 genomes] |
rs73279111 | 1.00[AMR][1000 genomes] |
rs73279124 | 1.00[AMR][1000 genomes] |
rs73279126 | 1.00[AMR][1000 genomes] |
rs73279129 | 1.00[AMR][1000 genomes] |
rs73279149 | 1.00[AMR][1000 genomes] |
rs73279151 | 1.00[AMR][1000 genomes] |
rs73279187 | 1.00[AMR][1000 genomes] |
rs73281085 | 1.00[AMR][1000 genomes] |
rs73283042 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73284986 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73287008 | 1.00[AMR][1000 genomes] |
rs73287009 | 1.00[AMR][1000 genomes] |
rs73288937 | 1.00[AMR][1000 genomes] |
rs73288940 | 1.00[AMR][1000 genomes] |
rs73288992 | 1.00[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv899049 | chr12:45299202-45376053 | Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats | TF binding regionCpG islandChromatin interactive region | 4 gene(s) | inside rSNPs | diseases |
2 | nsv899050 | chr12:45299202-45400614 | Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive region | 4 gene(s) | inside rSNPs | diseases |
3 | nsv899051 | chr12:45307633-45376053 | Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive region | 4 gene(s) | inside rSNPs | diseases |
No data |