Variant report
Variant | rs4556111 |
---|---|
Chromosome Location | chr8:113382838-113382839 |
allele | C/T |
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] |
---|---|
rs10098649 | 0.84[YRI][hapmap] |
rs10156319 | 0.85[YRI][hapmap] |
rs12156373 | 0.85[CEU][hapmap] |
rs12681029 | 0.81[CHD][hapmap];0.90[JPT][hapmap] |
rs1303762 | 1.00[CEU][hapmap];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs1388965 | 0.88[MEX][hapmap];0.81[TSI][hapmap] |
rs1420851 | 0.81[CEU][hapmap] |
rs1420854 | 0.88[MEX][hapmap] |
rs1420858 | 0.89[CEU][hapmap] |
rs1420859 | 0.93[CEU][hapmap];0.87[MEX][hapmap];0.87[EUR][1000 genomes] |
rs1492674 | 0.85[CEU][hapmap] |
rs1492678 | 0.81[TSI][hapmap] |
rs16883388 | 0.85[YRI][hapmap] |
rs1873746 | 0.84[MEX][hapmap];0.81[TSI][hapmap] |
rs1895014 | 0.80[CEU][hapmap] |
rs2016614 | 1.00[CEU][hapmap];0.96[MEX][hapmap];0.91[TSI][hapmap];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs2131298 | 0.88[MEX][hapmap] |
rs2172352 | 0.92[CEU][hapmap] |
rs28453001 | 0.82[EUR][1000 genomes] |
rs28688503 | 0.89[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs3950676 | 0.80[MEX][hapmap];0.81[TSI][hapmap] |
rs41340951 | 0.84[MEX][hapmap] |
rs4143627 | 0.81[CEU][hapmap];0.88[MEX][hapmap] |
rs41467949 | 0.83[MEX][hapmap];0.81[TSI][hapmap] |
rs4563913 | 0.88[MEX][hapmap];0.81[TSI][hapmap] |
rs4601350 | 0.93[CEU][hapmap];0.83[EUR][1000 genomes] |
rs4876281 | 0.92[CEU][hapmap];0.85[TSI][hapmap] |
rs4876468 | 0.81[TSI][hapmap] |
rs6469413 | 0.80[MEX][hapmap];0.81[TSI][hapmap] |
rs6469414 | 0.87[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs7000912 | 0.88[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs7003500 | 0.81[TSI][hapmap] |
rs7826278 | 0.87[EUR][1000 genomes] |
rs7845628 | 0.85[CEU][hapmap];0.92[MEX][hapmap];0.82[EUR][1000 genomes] |
rs7845794 | 0.93[CEU][hapmap];0.83[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs929685 | 0.93[CEU][hapmap];0.87[EUR][1000 genomes] |
rs929687 | 0.86[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv533857 | chr8:112819659-113801258 | Enhancers Bivalent Enhancer Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 9 gene(s) | inside rSNPs | diseases |
2 | nsv1022457 | chr8:113071774-113811177 | Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 6 gene(s) | inside rSNPs | diseases |
3 | esv2755868 | chr8:113282795-113634842 | Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
4 | esv2753595 | chr8:113283214-114190390 | Enhancers Weak transcription Active TSS Strong transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 6 gene(s) | inside rSNPs | diseases |
5 | esv2754232 | chr8:113294967-113634842 | Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
6 | nsv891323 | chr8:113359377-113394699 | Weak transcription Enhancers ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | n/a |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:113382000-113383200 | Weak transcription | Pancreas | Pancrea |