Variant report
Variant | rs71428189 |
---|---|
Chromosome Location | chr2:125967214-125967215 |
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] |
---|---|
rs12992489 | 1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs12995266 | 1.00[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs13006314 | 0.82[AMR][1000 genomes] |
rs13014302 | 0.86[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs13024027 | 1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs13024249 | 0.86[AMR][1000 genomes] |
rs13025135 | 0.90[AMR][1000 genomes] |
rs13025656 | 0.86[AMR][1000 genomes] |
rs13033685 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs17629296 | 0.86[AMR][1000 genomes] |
rs34099871 | 0.86[AMR][1000 genomes] |
rs34250117 | 1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs34308133 | 1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs34321799 | 0.86[AMR][1000 genomes] |
rs34321922 | 0.86[AMR][1000 genomes] |
rs34495630 | 1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs34693807 | 0.86[AMR][1000 genomes] |
rs34870179 | 0.86[AMR][1000 genomes] |
rs34961659 | 0.86[AMR][1000 genomes] |
rs35120173 | 0.90[AMR][1000 genomes] |
rs35318750 | 0.86[AMR][1000 genomes] |
rs35355440 | 0.86[AMR][1000 genomes] |
rs35364524 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs35878249 | 0.86[AMR][1000 genomes] |
rs36108797 | 0.95[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs71428174 | 1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs71428188 | 0.95[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs71428190 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs71428193 | 0.90[AMR][1000 genomes];0.81[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv431646 | chr2:125780602-126174341 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers | TF binding regionChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
2 | nsv874992 | chr2:125817682-126046421 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats | TF binding regionChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
3 | nsv999840 | chr2:125902993-126683646 | Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
4 | nsv1012762 | chr2:125902993-126755660 | Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
5 | nsv535915 | chr2:125902993-126755660 | ZNF genes & repeats Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
6 | nsv1001555 | chr2:125904415-126630781 | Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
7 | nsv535916 | chr2:125904415-126630781 | Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:125966800-125968000 | Enhancers | H9 Cell Line | embryonic stem cell |
2 | chr2:125967000-125967800 | Enhancers | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |