Variant report

Variant	rs10112206
Chromosome Location	chr8:65611761-65611762
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:65610299..65612672-chr8:65616238..65617888,2	K562	blood:

Extended variants
information (count: 43 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10081461	0.95[CHB][hapmap];0.82[JPT][hapmap];0.81[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs10090584	0.95[CHB][hapmap];0.82[JPT][hapmap];0.90[ASN][1000 genomes]
rs10092618	0.95[CHB][hapmap];0.88[ASN][1000 genomes]
rs10105184	0.95[CHB][hapmap];0.87[ASN][1000 genomes]
rs10808738	0.95[CHB][hapmap];0.95[CHD][hapmap];0.92[MEX][hapmap];0.87[ASN][1000 genomes]
rs10957321	0.92[CEU][hapmap];1.00[CHB][hapmap];0.90[CHD][hapmap];0.91[JPT][hapmap];0.84[MEX][hapmap];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11986615	0.95[CHB][hapmap];0.90[ASN][1000 genomes]
rs11995512	0.95[ASN][1000 genomes]
rs11998077	0.95[CHB][hapmap];0.95[CHD][hapmap];0.81[GIH][hapmap];0.82[JPT][hapmap];1.00[MEX][hapmap];0.95[ASN][1000 genomes]
rs12548518	1.00[CEU][hapmap];0.97[CHD][hapmap];0.89[GIH][hapmap];0.95[JPT][hapmap];0.87[MEX][hapmap];0.93[TSI][hapmap];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12681856	0.89[ASN][1000 genomes]
rs13252547	1.00[CEU][hapmap];0.95[CHB][hapmap];0.97[CHD][hapmap];0.87[GIH][hapmap];0.95[JPT][hapmap];0.96[MEX][hapmap];1.00[TSI][hapmap];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13260704	0.90[ASN][1000 genomes]
rs1986181	0.95[CHB][hapmap];0.82[JPT][hapmap];0.90[ASN][1000 genomes]
rs28679790	0.86[ASN][1000 genomes]
rs4236934	0.95[CHB][hapmap];0.84[CHD][hapmap];0.87[ASN][1000 genomes]
rs4327886	0.95[CHB][hapmap];0.84[CHD][hapmap];0.85[ASN][1000 genomes]
rs4395923	0.95[CHB][hapmap];0.95[CHD][hapmap];0.92[MEX][hapmap]
rs4406437	0.95[CHB][hapmap];0.95[CHD][hapmap];0.81[GIH][hapmap];0.82[JPT][hapmap];1.00[MEX][hapmap];0.95[ASN][1000 genomes]
rs4437694	0.90[ASN][1000 genomes]
rs4452822	0.95[CHB][hapmap];0.95[CHD][hapmap];0.92[MEX][hapmap];0.86[ASN][1000 genomes]
rs4461935	0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4486246	0.95[CHB][hapmap];0.84[CHD][hapmap];0.88[ASN][1000 genomes]
rs4507804	0.95[CHB][hapmap]
rs4532631	0.90[ASN][1000 genomes]
rs4549814	0.90[ASN][1000 genomes]
rs4581093	0.95[CHB][hapmap];0.95[CHD][hapmap];0.92[MEX][hapmap];0.87[ASN][1000 genomes]
rs4737198	0.85[ASN][1000 genomes]
rs6472147	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6999999	0.95[CHB][hapmap];0.95[CHD][hapmap];0.96[MEX][hapmap];0.90[ASN][1000 genomes]
rs7004685	0.95[CHB][hapmap]
rs7005708	0.95[CHB][hapmap];0.84[CHD][hapmap];0.86[ASN][1000 genomes]
rs7815372	1.00[CHB][hapmap];0.82[CHD][hapmap];0.90[JPT][hapmap];0.95[ASN][1000 genomes]
rs7817744	0.95[CHB][hapmap];0.84[CHD][hapmap];0.82[JPT][hapmap];0.90[ASN][1000 genomes]
rs7827287	0.96[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];0.91[JPT][hapmap];1.00[MEX][hapmap];0.91[TSI][hapmap];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7830315	0.92[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];0.91[JPT][hapmap];0.96[MEX][hapmap];0.89[TSI][hapmap];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7834854	0.95[CHB][hapmap];0.82[JPT][hapmap];0.90[ASN][1000 genomes]
rs7842714	0.80[EUR][1000 genomes]
rs9298086	0.83[MEX][hapmap]
rs9298087	0.95[CHB][hapmap];0.95[CHD][hapmap];0.92[MEX][hapmap];0.88[ASN][1000 genomes]
rs9298088	0.95[CHB][hapmap];0.95[CHD][hapmap];0.92[MEX][hapmap];0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv534001	chr8:64992196-65798776	Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases
2	esv2761434	chr8:65578467-66567678	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs10112206	CYP7B1	cis	cerebellum	SCAN
rs10112206	CYP7B1	cis	parietal	SCAN
rs10112206	CHD7	cis	cerebellum	SCAN

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:65605600-65615200	Weak transcription	Aorta	Aorta
2	chr8:65606000-65612600	Weak transcription	Pancreas	Pancrea
3	chr8:65606000-65612600	Weak transcription	Spleen	Spleen
4	chr8:65608000-65612200	Weak transcription	Fetal Brain Female	brain
5	chr8:65608000-65612400	Weak transcription	Brain Anterior Caudate	brain
6	chr8:65608000-65612400	Weak transcription	Brain Hippocampus Middle	brain
7	chr8:65608000-65612600	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr8:65608200-65612600	Weak transcription	Brain Substantia Nigra	brain
9	chr8:65608800-65612600	Weak transcription	Brain Angular Gyrus	brain
10	chr8:65610000-65611800	Enhancers	Placenta Amnion	Placenta Amnion
11	chr8:65610200-65611800	Enhancers	Liver	Liver
12	chr8:65610400-65612600	Weak transcription	Fetal Brain Male	brain
13	chr8:65611400-65612000	Enhancers	GM12878-XiMat	blood
14	chr8:65611600-65611800	Enhancers	Brain Cingulate Gyrus	brain

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