Variant report
Variant | rs10756676 |
---|---|
Chromosome Location | chr9:15599101-15599102 |
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] |
---|---|
rs1039813 | 0.87[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs1039814 | 0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs10481557 | 0.82[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs10738400 | 0.82[EUR][1000 genomes] |
rs10738402 | 0.89[EUR][1000 genomes] |
rs10738404 | 0.83[EUR][1000 genomes] |
rs10738405 | 0.82[EUR][1000 genomes] |
rs10738406 | 0.82[EUR][1000 genomes] |
rs10756670 | 0.81[EUR][1000 genomes] |
rs10756671 | 0.82[EUR][1000 genomes] |
rs10756672 | 0.83[EUR][1000 genomes] |
rs10756674 | 0.87[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs10756677 | 0.84[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs10756678 | 0.86[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs10756679 | 0.90[EUR][1000 genomes] |
rs10756680 | 0.91[EUR][1000 genomes] |
rs10756686 | 0.89[EUR][1000 genomes] |
rs10756687 | 0.84[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs10756688 | 0.91[EUR][1000 genomes] |
rs10756689 | 0.91[EUR][1000 genomes] |
rs10756690 | 0.86[EUR][1000 genomes] |
rs10756692 | 0.81[EUR][1000 genomes] |
rs10756694 | 0.83[EUR][1000 genomes] |
rs10756695 | 0.82[EUR][1000 genomes] |
rs10756696 | 0.80[EUR][1000 genomes] |
rs10810399 | 0.89[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs10810400 | 0.89[EUR][1000 genomes] |
rs10810401 | 0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs10810402 | 0.92[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs10810405 | 0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs10810407 | 0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs10810408 | 0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs10810409 | 0.92[EUR][1000 genomes] |
rs10810410 | 0.87[EUR][1000 genomes] |
rs10810416 | 0.81[EUR][1000 genomes] |
rs10810419 | 0.81[EUR][1000 genomes] |
rs10810428 | 0.85[EUR][1000 genomes] |
rs10810431 | 0.83[EUR][1000 genomes] |
rs10810432 | 0.83[EUR][1000 genomes] |
rs10810433 | 0.82[EUR][1000 genomes] |
rs10810434 | 0.82[EUR][1000 genomes] |
rs10810435 | 0.81[EUR][1000 genomes] |
rs10810436 | 0.80[EUR][1000 genomes] |
rs10962064 | 0.82[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs10962065 | 0.81[EUR][1000 genomes] |
rs10962066 | 0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs10962070 | 0.90[EUR][1000 genomes] |
rs10962072 | 0.87[EUR][1000 genomes] |
rs10962073 | 0.86[EUR][1000 genomes] |
rs10962098 | 0.86[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs10962099 | 0.88[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs10962110 | 0.90[EUR][1000 genomes] |
rs10962124 | 0.81[EUR][1000 genomes] |
rs11789563 | 0.83[EUR][1000 genomes] |
rs11791627 | 0.81[EUR][1000 genomes] |
rs11792937 | 0.81[EUR][1000 genomes] |
rs12340969 | 0.91[EUR][1000 genomes] |
rs13291638 | 0.92[EUR][1000 genomes] |
rs13301516 | 0.81[EUR][1000 genomes] |
rs1396707 | 0.82[EUR][1000 genomes] |
rs1396708 | 0.82[EUR][1000 genomes] |
rs1509310 | 0.81[EUR][1000 genomes] |
rs1533040 | 0.84[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs1553728 | 0.87[EUR][1000 genomes] |
rs1812686 | 0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs2055772 | 0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs2136355 | 0.83[EUR][1000 genomes] |
rs2175082 | 0.82[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs2382532 | 0.83[EUR][1000 genomes] |
rs2382534 | 0.82[EUR][1000 genomes] |
rs2382538 | 0.82[EUR][1000 genomes] |
rs2457265 | 0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs276447 | 0.81[ASN][1000 genomes] |
rs276448 | 0.80[ASN][1000 genomes] |
rs276454 | 0.89[ASN][1000 genomes] |
rs276455 | 0.95[ASN][1000 genomes] |
rs3955162 | 0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs4281189 | 0.87[EUR][1000 genomes] |
rs432452 | 0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs4339736 | 0.85[EUR][1000 genomes] |
rs440229 | 0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs4448380 | 0.94[EUR][1000 genomes] |
rs451878 | 0.80[EUR][1000 genomes] |
rs4740614 | 0.82[ASN][1000 genomes] |
rs4740615 | 0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs4740618 | 0.90[EUR][1000 genomes] |
rs4740619 | 0.93[EUR][1000 genomes] |
rs4740620 | 0.83[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs4740621 | 0.82[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs4740622 | 0.82[EUR][1000 genomes] |
rs4741510 | 0.84[EUR][1000 genomes] |
rs4741512 | 0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs4741515 | 0.83[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs4741517 | 0.83[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs4741519 | 0.83[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs4741520 | 0.88[EUR][1000 genomes] |
rs4741527 | 0.81[EUR][1000 genomes] |
rs4741528 | 0.91[EUR][1000 genomes] |
rs4741529 | 0.90[EUR][1000 genomes] |
rs4741534 | 0.82[EUR][1000 genomes] |
rs6474931 | 0.83[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs6474942 | 0.88[EUR][1000 genomes] |
rs6474944 | 0.87[EUR][1000 genomes] |
rs6474945 | 0.88[EUR][1000 genomes] |
rs6474953 | 0.82[EUR][1000 genomes] |
rs6474954 | 0.82[EUR][1000 genomes] |
rs6474955 | 0.82[EUR][1000 genomes] |
rs7020760 | 0.82[EUR][1000 genomes] |
rs7024640 | 0.82[EUR][1000 genomes] |
rs7025669 | 0.91[EUR][1000 genomes] |
rs7032755 | 0.88[EUR][1000 genomes] |
rs7032877 | 0.88[EUR][1000 genomes] |
rs7036172 | 0.91[EUR][1000 genomes] |
rs7036674 | 0.91[EUR][1000 genomes] |
rs7042475 | 0.81[EUR][1000 genomes] |
rs7044122 | 0.84[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs7049101 | 0.87[EUR][1000 genomes] |
rs7049176 | 0.87[EUR][1000 genomes] |
rs7389023 | 0.82[EUR][1000 genomes] |
rs7389047 | 0.91[EUR][1000 genomes] |
rs7389629 | 0.87[EUR][1000 genomes] |
rs770524 | 0.81[ASN][1000 genomes] |
rs7847144 | 0.82[EUR][1000 genomes] |
rs7854714 | 0.86[EUR][1000 genomes] |
rs7855235 | 0.82[EUR][1000 genomes] |
rs7859780 | 0.93[EUR][1000 genomes] |
rs7860623 | 0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs7861004 | 0.82[EUR][1000 genomes] |
rs7863088 | 0.93[EUR][1000 genomes] |
rs7873152 | 0.84[ASN][1000 genomes] |
rs7874533 | 0.86[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs7875367 | 0.83[ASN][1000 genomes] |
rs9407624 | 0.83[ASN][1000 genomes] |
rs9650677 | 0.81[EUR][1000 genomes] |
rs9696751 | 0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9886779 | 0.88[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv892625 | chr9:15326251-16064850 | Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 35 gene(s) | inside rSNPs | diseases |
2 | nsv892626 | chr9:15389610-15694690 | Flanking Active TSS Active TSS Weak transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 27 gene(s) | inside rSNPs | diseases |
3 | nsv892627 | chr9:15397969-15909450 | Enhancers Flanking Active TSS Strong transcription Weak transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 28 gene(s) | inside rSNPs | diseases |
4 | nsv892629 | chr9:15516375-15634326 | Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
5 | esv3407839 | chr9:15530438-15665653 | Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
6 | nsv892630 | chr9:15554960-15694690 | Weak transcription Strong transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Genic enhancers | TF binding regionChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
7 | nsv1028357 | chr9:15565670-15622556 | Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS | TF binding regionChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
8 | esv2752286 | chr9:15578017-15794897 | Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS | TF binding regionChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
9 | nsv613652 | chr9:15579744-15661859 | Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Active TSS | TF binding regionChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
10 | nsv613653 | chr9:15590116-15668606 | Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers | Chromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
11 | nsv892631 | chr9:15590116-15694690 | Weak transcription ZNF genes & repeats Genic enhancers Enhancers Strong transcription Flanking Active TSS Active TSS | Chromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
12 | nsv892632 | chr9:15590116-15869845 | Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr9:15587000-15620400 | Weak transcription | Pancreas | Pancrea |
2 | chr9:15588600-15600800 | Weak transcription | Primary hematopoietic stem cells short term culture | blood |
3 | chr9:15588600-15601000 | Weak transcription | Breast Myoepithelial Primary Cells | Breast |
4 | chr9:15589200-15609800 | Weak transcription | Sigmoid Colon | Sigmoid Colon |
5 | chr9:15589400-15610600 | Weak transcription | Thymus | Thymus |
6 | chr9:15592800-15600600 | Weak transcription | Fetal Thymus | thymus |
7 | chr9:15592800-15614000 | Weak transcription | Left Ventricle | heart |
8 | chr9:15593000-15600800 | Weak transcription | H1 Cell Line | embryonic stem cell |
9 | chr9:15599000-15600200 | ZNF genes & repeats | Primary hematopoietic stem cells G-CSF-mobilized Female | -- |
10 | chr9:15599000-15601400 | ZNF genes & repeats | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |
11 | chr9:15599000-15617800 | Weak transcription | Aorta | Aorta |