Variant report

Variant	rs13248218
Chromosome Location	chr8:4811595-4811596
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:4805755..4808307-chr8:4809361..4811905,2	K562	blood:

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10088688	0.89[CEU][hapmap]
rs10094549	0.90[CEU][hapmap];0.82[CHB][hapmap];0.82[JPT][hapmap]
rs10101412	0.85[CEU][hapmap]
rs10105362	0.89[CEU][hapmap];0.81[CHB][hapmap];0.80[JPT][hapmap]
rs10110891	0.87[CHB][hapmap];0.82[JPT][hapmap];0.81[ASN][1000 genomes]
rs1011587	0.89[CEU][hapmap]
rs10503294	0.90[CEU][hapmap];0.96[CHB][hapmap];0.91[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10503296	0.90[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11136808	0.95[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap]
rs11136811	0.87[CHB][hapmap];0.82[ASN][1000 genomes]
rs11136813	0.87[CHB][hapmap];0.82[JPT][hapmap];0.82[ASN][1000 genomes]
rs11984699	0.96[CHB][hapmap];0.86[JPT][hapmap];0.86[ASN][1000 genomes]
rs12114470	0.90[CEU][hapmap];0.84[CHB][hapmap]
rs12155630	0.90[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12541020	0.82[CHB][hapmap];0.81[JPT][hapmap];0.82[ASN][1000 genomes]
rs12545626	0.90[CEU][hapmap]
rs12674915	0.90[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13254311	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap]
rs13264559	0.89[CEU][hapmap]
rs13273154	1.00[CEU][hapmap];0.82[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap]
rs2924719	0.80[CEU][hapmap]
rs2924720	0.89[CEU][hapmap]
rs2924723	0.89[CEU][hapmap]
rs2924724	0.89[CEU][hapmap]
rs2977732	0.84[CEU][hapmap]
rs2977733	0.85[CEU][hapmap]
rs4076510	0.85[CEU][hapmap]
rs4272399	0.80[EUR][1000 genomes]
rs4278171	0.84[CEU][hapmap]
rs4295679	0.90[CEU][hapmap];0.96[CHB][hapmap];0.91[JPT][hapmap]
rs4329292	0.90[CEU][hapmap]
rs4360313	0.90[CEU][hapmap];0.87[CHB][hapmap];0.91[JPT][hapmap];1.00[YRI][hapmap]
rs4385481	0.90[CEU][hapmap];0.82[CHB][hapmap];0.82[JPT][hapmap];1.00[YRI][hapmap]
rs4436145	0.80[EUR][1000 genomes]
rs4477045	0.85[CEU][hapmap]
rs4495447	0.90[CEU][hapmap]
rs4517142	0.89[CEU][hapmap];0.81[EUR][1000 genomes]
rs4517143	0.89[CEU][hapmap];0.81[EUR][1000 genomes]
rs4593565	0.90[CEU][hapmap]
rs4614018	0.90[CEU][hapmap]
rs4623447	0.90[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4636228	0.86[ASN][1000 genomes]
rs4875426	0.89[CEU][hapmap];0.81[EUR][1000 genomes]
rs4875427	0.89[CEU][hapmap]
rs6558950	0.82[ASN][1000 genomes]
rs6558951	0.89[CEU][hapmap]
rs6986895	0.87[CHB][hapmap];0.81[JPT][hapmap]
rs6987219	0.87[JPT][hapmap]
rs7005677	0.91[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs7464891	0.82[CHB][hapmap];0.81[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv609876	chr8:4494811-5092970	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1029480	chr8:4497596-5081032	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv498130	chr8:4532988-5176376	Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Weak transcription Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv889976	chr8:4750266-4824335	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv1028542	chr8:4758159-4824005	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv1031026	chr8:4771072-5054326	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv889977	chr8:4802438-4820177	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:4811200-4811600	Enhancers	Fetal Intestine Large	intestine
2	chr8:4811200-4811600	Enhancers	Fetal Intestine Small	intestine
3	chr8:4811200-4813000	Enhancers	Adipose Nuclei	Adipose
4	chr8:4811400-4811600	Enhancers	Liver	Liver
5	chr8:4811400-4811800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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