Variant report
Variant | rs926102 |
---|---|
Chromosome Location | chr7:152762916-152762917 |
allele | A/G |
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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rs_ID | r2[population] |
---|---|
rs10227264 | 0.82[ASN][1000 genomes] |
rs10235625 | 1.00[JPT][hapmap] |
rs10254175 | 1.00[JPT][hapmap] |
rs10267720 | 1.00[JPT][hapmap] |
rs11489469 | 0.95[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap] |
rs1474497 | 0.95[CHB][hapmap];1.00[JPT][hapmap] |
rs1525038 | 1.00[JPT][hapmap] |
rs1525039 | 1.00[JPT][hapmap];0.87[ASN][1000 genomes] |
rs2037929 | 0.98[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes] |
rs2205168 | 0.95[ASN][1000 genomes] |
rs2311857 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs4265104 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs4448172 | 0.95[CHB][hapmap];0.95[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes] |
rs479215 | 0.84[ASN][1000 genomes] |
rs5029723 | 0.95[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap] |
rs510588 | 0.86[ASN][1000 genomes] |
rs582492 | 1.00[JPT][hapmap] |
rs631720 | 0.98[ASN][1000 genomes] |
rs6464302 | 0.95[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes] |
rs671677 | 0.84[ASN][1000 genomes] |
rs678338 | 0.90[ASN][1000 genomes] |
rs760223 | 0.95[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes] |
rs760224 | 0.86[CHB][hapmap];0.94[ASN][1000 genomes] |
rs760225 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes] |
rs972702 | 0.94[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1027100 | chr7:152294734-152935140 | Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 39 gene(s) | inside rSNPs | diseases |
2 | nsv532221 | chr7:152371297-152884547 | Weak transcription Strong transcription Flanking Bivalent TSS/Enh Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 31 gene(s) | inside rSNPs | diseases |
3 | nsv868873 | chr7:152371297-152900113 | Weak transcription Enhancers Bivalent/Poised TSS Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 31 gene(s) | inside rSNPs | diseases |
4 | nsv532222 | chr7:152504090-153450290 | Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 23 gene(s) | inside rSNPs | diseases |
5 | nsv1034937 | chr7:152566162-152854895 | Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
6 | nsv831194 | chr7:152762400-152963937 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr7:152762200-152763400 | Weak transcription | Pancreas | Pancrea |