Variant report

Variant	rs8000315
Chromosome Location	chr13:93490840-93490841
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs12428589	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12429124	1.00[MEX][hapmap];0.85[AMR][1000 genomes]
rs12429680	1.00[CHB][hapmap];0.97[CHD][hapmap];0.94[JPT][hapmap]
rs12431303	1.00[CHB][hapmap];0.87[JPT][hapmap]
rs1590556	0.96[ASN][1000 genomes]
rs1890198	1.00[CHB][hapmap];0.94[JPT][hapmap]
rs2031585	0.95[CHB][hapmap]
rs2148225	1.00[CHB][hapmap]
rs2182367	1.00[CHB][hapmap];0.94[JPT][hapmap]
rs35226443	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6492628	0.82[ASN][1000 genomes]
rs7321917	0.90[MEX][hapmap]
rs7333121	1.00[CHB][hapmap];0.94[JPT][hapmap]
rs7338330	0.90[MEX][hapmap]
rs7984465	0.83[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs7988257	0.95[CHB][hapmap];0.82[CHD][hapmap]
rs9556211	0.90[MEX][hapmap]
rs9556215	1.00[CHB][hapmap];0.94[JPT][hapmap]
rs9556216	0.95[CHB][hapmap];0.93[JPT][hapmap];0.96[ASN][1000 genomes]
rs9556217	1.00[CHB][hapmap];0.93[JPT][hapmap];0.96[ASN][1000 genomes]
rs9556218	1.00[CHB][hapmap];0.97[CHD][hapmap];0.94[JPT][hapmap];0.96[ASN][1000 genomes]
rs9556219	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9556222	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9556224	0.85[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs9556227	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9556228	1.00[CHB][hapmap];0.94[JPT][hapmap];0.99[ASN][1000 genomes]
rs9556229	1.00[CHB][hapmap];0.97[CHD][hapmap];0.94[JPT][hapmap]
rs9561131	0.85[AMR][1000 genomes]
rs9561143	0.90[MEX][hapmap];0.80[AMR][1000 genomes]
rs9561151	1.00[CHB][hapmap];0.92[JPT][hapmap]
rs9561152	1.00[CHB][hapmap];0.94[JPT][hapmap]
rs9561163	1.00[CHB][hapmap];0.94[JPT][hapmap]
rs9561164	0.97[ASN][1000 genomes]
rs9561165	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9561166	1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap]
rs9561168	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9561169	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs9561170	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9561172	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9561173	1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap]
rs9561175	0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9561176	0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9561177	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9561178	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs9561179	1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.90[MEX][hapmap]
rs9561180	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9561181	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9561182	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9561183	1.00[CHB][hapmap];0.94[CHD][hapmap];0.94[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869070	chr13:93347616-94286933	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv456072	chr13:93419362-93506864	Active TSS Flanking Active TSS Enhancers Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv562746	chr13:93419362-93506864	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv900907	chr13:93472377-93597799	Genic enhancers Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:93490400-93491800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr13:93490400-93491800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr13:93490600-93491400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr13:93490800-93491000	Enhancers	HMEC	breast
5	chr13:93490800-93491200	Enhancers	HSMM	muscle
6	chr13:93490800-93491600	Enhancers	NH-A	brain
7	chr13:93490800-93491800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr13:93490800-93491800	Enhancers	Osteobl	bone
9	chr13:93490800-93492000	Enhancers	Muscle Satellite Cultured Cells	--

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