Variant report

Variant	rs10086105
Chromosome Location	chr8:4188180-4188181
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10046757	0.81[EUR][1000 genomes]
rs10091031	0.89[CEU][hapmap];0.89[GIH][hapmap];0.87[JPT][hapmap];0.92[TSI][hapmap];0.84[EUR][1000 genomes]
rs10091134	0.89[CEU][hapmap];0.93[GIH][hapmap];0.87[JPT][hapmap];0.90[TSI][hapmap];0.84[EUR][1000 genomes]
rs10094349	0.89[CEU][hapmap];0.91[GIH][hapmap];0.87[JPT][hapmap];0.88[TSI][hapmap];0.82[EUR][1000 genomes]
rs10096058	0.82[JPT][hapmap]
rs10103498	0.85[CEU][hapmap];0.90[CHB][hapmap];0.94[CHD][hapmap];0.95[GIH][hapmap];0.88[JPT][hapmap];0.92[MEX][hapmap];0.90[TSI][hapmap];0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10103601	0.83[EUR][1000 genomes]
rs10103842	0.83[EUR][1000 genomes]
rs10103969	0.88[CEU][hapmap];0.87[JPT][hapmap];0.84[EUR][1000 genomes]
rs10104209	0.89[CEU][hapmap];0.91[CHD][hapmap];0.93[GIH][hapmap];0.90[TSI][hapmap];0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10104718	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10105113	0.88[JPT][hapmap]
rs10105349	0.80[JPT][hapmap]
rs10107472	0.85[CHB][hapmap];0.91[CHD][hapmap];0.88[JPT][hapmap];0.92[ASN][1000 genomes]
rs10108270	0.88[JPT][hapmap]
rs10108725	0.85[CHB][hapmap];0.91[CHD][hapmap];0.88[JPT][hapmap];0.91[ASN][1000 genomes]
rs10108980	0.88[ASN][1000 genomes]
rs10866968	0.90[CHB][hapmap];0.97[CHD][hapmap];0.94[JPT][hapmap];0.95[ASN][1000 genomes]
rs10866969	0.96[ASN][1000 genomes]
rs11136730	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11136731	0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12675938	0.87[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12679965	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs13268424	0.85[CHB][hapmap];0.88[JPT][hapmap];0.92[ASN][1000 genomes]
rs1504754	0.81[CHB][hapmap];0.81[CHD][hapmap];0.82[JPT][hapmap]
rs1546356	0.84[EUR][1000 genomes]
rs1847570	0.89[CEU][hapmap];0.91[GIH][hapmap];0.85[MEX][hapmap];0.88[TSI][hapmap];0.81[EUR][1000 genomes]
rs1875897	0.94[CHD][hapmap];0.85[TSI][hapmap];0.84[EUR][1000 genomes]
rs4875336	0.85[CHB][hapmap];0.82[JPT][hapmap];0.90[ASN][1000 genomes]
rs6558864	0.88[JPT][hapmap]
rs6558865	0.87[JPT][hapmap]
rs7015864	0.82[JPT][hapmap]
rs9314526	0.88[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949269	chr8:3556145-4246903	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
2	nsv530863	chr8:3710810-4381378	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv530531	chr8:3942575-4605088	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv1034771	chr8:3969767-4255716	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv889939	chr8:4033186-4718648	Enhancers ZNF genes & repeats Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv1032488	chr8:4072826-4328057	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv1019677	chr8:4095786-4328057	Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv1015485	chr8:4127704-4272847	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
9	esv34054	chr8:4165205-4450873	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
10	nsv889946	chr8:4185227-4192206	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
11	nsv438021	chr8:4185750-4196180	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:4171000-4188800	Weak transcription	Pancreas	Pancrea
2	chr8:4187800-4189800	Enhancers	Fetal Intestine Large	intestine

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