Variant report
Variant | rs6915295 |
---|---|
Chromosome Location | chr6:119783158-119783159 |
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] |
---|---|
rs1112369 | 0.89[EUR][1000 genomes] |
rs11153823 | 0.86[CHB][hapmap] |
rs11153828 | 0.89[EUR][1000 genomes] |
rs12195597 | 0.87[ASN][1000 genomes] |
rs12199966 | 0.87[ASN][1000 genomes] |
rs12202672 | 0.87[ASN][1000 genomes] |
rs12660903 | 0.81[EUR][1000 genomes] |
rs12661049 | 0.83[EUR][1000 genomes] |
rs1288077 | 0.92[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1288080 | 0.82[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs1288081 | 0.82[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs1318271 | 0.92[EUR][1000 genomes] |
rs1344333 | 0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1353864 | 0.89[EUR][1000 genomes] |
rs1392088 | 0.87[ASN][1000 genomes] |
rs1392090 | 0.89[EUR][1000 genomes] |
rs1499569 | 0.85[EUR][1000 genomes] |
rs1553171 | 0.89[EUR][1000 genomes] |
rs17081283 | 0.89[EUR][1000 genomes] |
rs17081375 | 0.83[EUR][1000 genomes] |
rs17081423 | 0.88[CEU][hapmap];0.84[JPT][hapmap];0.83[EUR][1000 genomes] |
rs1875056 | 0.91[EUR][1000 genomes] |
rs1963055 | 0.89[EUR][1000 genomes] |
rs2066353 | 0.92[EUR][1000 genomes] |
rs2153823 | 1.00[CEU][hapmap];0.84[JPT][hapmap];0.89[EUR][1000 genomes] |
rs2185752 | 0.92[EUR][1000 genomes] |
rs2357380 | 0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs3891962 | 0.94[EUR][1000 genomes] |
rs4142806 | 0.88[CEU][hapmap];0.81[JPT][hapmap];0.83[EUR][1000 genomes] |
rs4551205 | 0.83[EUR][1000 genomes] |
rs4613849 | 0.83[EUR][1000 genomes] |
rs4945640 | 0.89[EUR][1000 genomes] |
rs4945642 | 0.83[EUR][1000 genomes] |
rs4946417 | 0.82[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs4946418 | 0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4946420 | 0.92[EUR][1000 genomes] |
rs4946426 | 0.83[EUR][1000 genomes] |
rs4946427 | 0.88[CEU][hapmap];0.80[JPT][hapmap];0.83[EUR][1000 genomes] |
rs56081039 | 0.83[EUR][1000 genomes] |
rs56091753 | 0.83[EUR][1000 genomes] |
rs6569081 | 0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6569083 | 0.87[ASN][1000 genomes] |
rs6918211 | 0.89[EUR][1000 genomes] |
rs6923080 | 0.89[EUR][1000 genomes] |
rs6923700 | 0.87[ASN][1000 genomes] |
rs6935310 | 0.96[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs6940248 | 0.83[EUR][1000 genomes] |
rs7452780 | 0.83[EUR][1000 genomes] |
rs7738873 | 0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7745217 | 0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs904574 | 0.89[EUR][1000 genomes] |
rs9320693 | 0.87[ASN][1000 genomes] |
rs9320694 | 0.88[CEU][hapmap];0.84[JPT][hapmap];0.83[EUR][1000 genomes] |
rs9385073 | 0.89[EUR][1000 genomes] |
rs9385076 | 0.87[ASN][1000 genomes] |
rs9385077 | 0.87[ASN][1000 genomes] |
rs9387652 | 0.85[EUR][1000 genomes] |
rs9398513 | 0.90[CHB][hapmap] |
rs9398516 | 0.87[ASN][1000 genomes] |
rs9401151 | 0.87[ASN][1000 genomes] |
rs9481922 | 0.82[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs9481923 | 0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs9481924 | 0.82[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs9481927 | 0.96[EUR][1000 genomes] |
rs9481929 | 0.91[EUR][1000 genomes] |
rs9481930 | 0.91[EUR][1000 genomes] |
rs9481931 | 0.91[EUR][1000 genomes] |
rs9481933 | 0.89[EUR][1000 genomes] |
rs9481936 | 0.88[CEU][hapmap];0.81[JPT][hapmap];0.83[EUR][1000 genomes] |
rs9489714 | 0.82[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs9489715 | 0.96[EUR][1000 genomes] |
rs9489716 | 0.82[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs9489717 | 0.82[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs9489718 | 0.88[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs9489719 | 0.91[EUR][1000 genomes] |
rs9489720 | 0.89[EUR][1000 genomes] |
rs9489723 | 0.83[EUR][1000 genomes] |
rs9489724 | 0.81[EUR][1000 genomes] |
rs9489725 | 0.83[EUR][1000 genomes] |
rs9489727 | 0.83[EUR][1000 genomes] |
rs9489728 | 0.83[EUR][1000 genomes] |
rs9489729 | 0.83[EUR][1000 genomes] |
rs9489731 | 0.83[EUR][1000 genomes] |
rs9489733 | 0.88[CEU][hapmap];0.81[JPT][hapmap];0.83[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv3447598 | chr6:119558591-120119384 | Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 27 gene(s) | inside rSNPs | diseases |
2 | esv3389526 | chr6:119558598-120190087 | ZNF genes & repeats Enhancers Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 27 gene(s) | inside rSNPs | diseases |
3 | nsv1027904 | chr6:119709488-120001986 | Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Strong transcription | Chromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
4 | nsv533518 | chr6:119712186-119998618 | ZNF genes & repeats Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription | Chromatin interactive regionlncRNA | 10 gene(s) | inside rSNPs | diseases |
5 | esv3442553 | chr6:119742069-120076777 | Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription | Chromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:119776200-119789200 | Weak transcription | Fetal Heart | heart |
2 | chr6:119777600-119784200 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
3 | chr6:119781600-119783600 | ZNF genes & repeats | GM12878-XiMat | blood |
4 | chr6:119781600-119784200 | Weak transcription | Rectal Mucosa Donor 29 | rectum |
5 | chr6:119782000-119784000 | Weak transcription | Primary B cells from peripheral blood | blood |
6 | chr6:119782800-119783600 | ZNF genes & repeats | Primary hematopoietic stem cells | blood |