Variant report

Variant	rs160437
Chromosome Location	chr8:90681884-90681885
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:90671410..90674363-chr8:90680458..90682126,2	K562	blood:
2	chr8:90677064..90679784-chr8:90680421..90682775,2	MCF-7	breast:
3	chr8:90671410..90675466-chr8:90680458..90682318,3	K562	blood:

Extended variants
information (count: 60 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs10108588	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1032516	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1040327	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10956191	0.83[ASN][1000 genomes]
rs10956209	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12216864	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs13266524	0.84[EUR][1000 genomes]
rs13278061	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1603289	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs160423	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs160424	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs160427	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs160429	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs160441	0.82[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs160447	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs160448	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs160449	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs160450	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs160451	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs160453	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs183363	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2088198	0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2101854	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs216989	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs218882	0.85[EUR][1000 genomes]
rs218884	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs218885	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs218886	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs218887	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs218888	0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs218889	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs218890	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs218915	0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs218917	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.90[YRI][hapmap];0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs218918	0.93[CEU][hapmap];0.94[CHB][hapmap];0.94[JPT][hapmap];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs218943	0.80[EUR][1000 genomes]
rs218945	0.80[EUR][1000 genomes]
rs218950	0.80[EUR][1000 genomes]
rs2202990	0.82[EUR][1000 genomes]
rs28374917	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2840206	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs28819479	0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs34036322	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs419004	0.81[EUR][1000 genomes]
rs4961157	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4961159	0.84[EUR][1000 genomes]
rs56237088	0.84[EUR][1000 genomes]
rs56403153	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6981616	0.81[CHB][hapmap]
rs6999425	0.82[EUR][1000 genomes]
rs7003919	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7004089	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv465735	chr8:89760311-90729507	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
2	nsv611714	chr8:89760311-90729507	Enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Weak transcription Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
3	nsv870380	chr8:90546585-90720182	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
4	nsv982109	chr8:90556188-90703631	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
5	nsv1026523	chr8:90558935-90722580	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
6	nsv831389	chr8:90575517-90753120	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
7	nsv1017263	chr8:90605445-90722580	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
8	nsv1031578	chr8:90670102-90757821	Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs160437	RP11-37B2.1	cis	Nerve Tibial	GTEx
rs160437	RP11-37B2.1	cis	Skin Sun Exposed Lower leg	GTEx

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:90675800-90684800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:90676000-90690600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr8:90676000-90690600	Weak transcription	Pancreas	Pancrea
4	chr8:90677000-90684600	Weak transcription	Aorta	Aorta
5	chr8:90679800-90682400	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr8:90681000-90682200	Enhancers	Fetal Stomach	stomach
7	chr8:90681200-90682000	Enhancers	Colon Smooth Muscle	Colon
8	chr8:90681600-90682000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr8:90681600-90682000	Enhancers	Ovary	ovary
10	chr8:90681600-90682000	Enhancers	Right Atrium	heart

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