Variant report
Variant | rs10203323 |
---|---|
Chromosome Location | chr2:115516080-115516081 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
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(count:2 , 50 per page) page:
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rs_ID | r2[population] |
---|---|
rs1002872 | 1.00[ASN][1000 genomes] |
rs10211528 | 0.88[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs12463387 | 1.00[ASN][1000 genomes] |
rs12463533 | 1.00[ASN][1000 genomes] |
rs12478020 | 1.00[ASN][1000 genomes] |
rs12711803 | 1.00[ASN][1000 genomes] |
rs13010772 | 1.00[ASN][1000 genomes] |
rs13017277 | 1.00[ASN][1000 genomes] |
rs13022000 | 0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs13032093 | 1.00[ASN][1000 genomes] |
rs13386918 | 0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs13425488 | 1.00[ASN][1000 genomes] |
rs13430153 | 0.80[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17043351 | 1.00[ASN][1000 genomes] |
rs17043357 | 1.00[ASN][1000 genomes] |
rs17043364 | 1.00[ASN][1000 genomes] |
rs17729212 | 0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17729314 | 1.00[ASN][1000 genomes] |
rs17730230 | 1.00[ASN][1000 genomes] |
rs17786067 | 1.00[ASN][1000 genomes] |
rs35456562 | 1.00[ASN][1000 genomes] |
rs4569486 | 1.00[ASN][1000 genomes] |
rs71418511 | 1.00[ASN][1000 genomes] |
rs71418512 | 1.00[ASN][1000 genomes] |
rs71418517 | 0.85[AFR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72830390 | 0.96[AFR][1000 genomes] |
rs72955668 | 1.00[ASN][1000 genomes] |
rs7605779 | 0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs930314 | 1.00[ASN][1000 genomes] |
rs967034 | 1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv874904 | chr2:114751691-115605062 | Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 10 gene(s) | inside rSNPs | diseases |
2 | nsv431502 | chr2:115139566-115617936 | Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
3 | nsv431524 | chr2:115425650-115530770 | Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS | Chromatin interactive region | n/a | inside rSNPs | n/a |
4 | nsv582715 | chr2:115495142-115573499 | Enhancers Weak transcription Flanking Active TSS Active TSS | Chromatin interactive region | n/a | inside rSNPs | n/a |
5 | nsv459019 | chr2:115495142-115599013 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | n/a |
6 | nsv874907 | chr2:115515053-115532766 | Enhancers Weak transcription | Chromatin interactive region | n/a | inside rSNPs | n/a |
7 | nsv874908 | chr2:115515053-115535141 | Enhancers Weak transcription | Chromatin interactive region | n/a | inside rSNPs | n/a |
8 | nsv874909 | chr2:115515053-115536791 | Enhancers Weak transcription | Chromatin interactive region | n/a | inside rSNPs | n/a |
9 | nsv874910 | chr2:115515053-115543018 | Enhancers Weak transcription | Chromatin interactive region | n/a | inside rSNPs | n/a |
10 | nsv874911 | chr2:115515053-115554390 | Enhancers Weak transcription Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | n/a |
11 | nsv874912 | chr2:115516080-115536791 | Enhancers Weak transcription | Chromatin interactive region | n/a | inside rSNPs | n/a |
12 | nsv874913 | chr2:115516080-115542869 | Enhancers Weak transcription | Chromatin interactive region | n/a | inside rSNPs | n/a |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:115513200-115520800 | Weak transcription | Pancreas | Pancrea |