Variant report
Variant | rs7146908 |
---|---|
Chromosome Location | chr14:64784436-64784437 |
allele | C/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 |
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No data |
rs_ID | r2[population] |
---|---|
rs10136955 | 1.00[CEU][hapmap];1.00[EUR][1000 genomes] |
rs10137994 | 1.00[EUR][1000 genomes] |
rs10140457 | 0.84[EUR][1000 genomes] |
rs17101718 | 0.86[YRI][hapmap] |
rs17101774 | 1.00[CEU][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs28485225 | 0.92[EUR][1000 genomes] |
rs28499370 | 0.92[EUR][1000 genomes] |
rs28663685 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs3783735 | 0.85[EUR][1000 genomes] |
rs59216189 | 0.92[EUR][1000 genomes] |
rs73267889 | 1.00[EUR][1000 genomes] |
rs73269927 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73269936 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv902019 | chr14:64395569-64882380 | Enhancers Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 48 gene(s) | inside rSNPs | diseases |
2 | nsv1307 | chr14:64742037-64787315 | Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive region | 4 gene(s) | inside rSNPs | diseases |
No data |