Variant report

Variant	rs6981814
Chromosome Location	chr8:113410506-113410507
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 82 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:77)

rs_ID	r²[population]
rs10092138	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10101060	1.00[YRI][hapmap]
rs10107134	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10110469	1.00[YRI][hapmap]
rs10111988	1.00[CEU][hapmap];0.81[CHB][hapmap];1.00[YRI][hapmap];0.84[AMR][1000 genomes]
rs1019350	0.91[CEU][hapmap]
rs1021438	1.00[CEU][hapmap];0.85[CHB][hapmap]
rs10216803	1.00[CEU][hapmap];0.85[CHB][hapmap];1.00[YRI][hapmap]
rs10505174	1.00[CEU][hapmap];0.85[CHB][hapmap]
rs10505175	1.00[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];0.88[ASN][1000 genomes]
rs10505176	0.81[CEU][hapmap]
rs10955618	0.81[CEU][hapmap]
rs1158895	0.81[CEU][hapmap];1.00[YRI][hapmap]
rs11775013	0.81[CEU][hapmap]
rs11778155	1.00[YRI][hapmap]
rs11778209	0.81[CEU][hapmap]
rs11778262	0.81[CEU][hapmap]
rs11778532	1.00[YRI][hapmap]
rs11779960	1.00[CEU][hapmap];0.85[CHB][hapmap]
rs11783041	1.00[CEU][hapmap];0.88[CHB][hapmap];0.82[AMR][1000 genomes]
rs11785270	1.00[YRI][hapmap]
rs11785419	0.81[CEU][hapmap]
rs11787085	0.84[AMR][1000 genomes]
rs1319683	1.00[CHB][hapmap];0.91[JPT][hapmap];0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs13439841	0.85[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs1352995	1.00[CEU][hapmap];0.85[CHB][hapmap];1.00[YRI][hapmap]
rs1377368	1.00[YRI][hapmap]
rs1388962	0.92[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.83[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs1420857	1.00[YRI][hapmap]
rs1492675	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1548986	1.00[YRI][hapmap]
rs16883359	1.00[YRI][hapmap]
rs16883360	0.81[CEU][hapmap]
rs16883401	1.00[YRI][hapmap]
rs16883404	1.00[YRI][hapmap]
rs16883432	1.00[YRI][hapmap]
rs16883437	0.81[CEU][hapmap];1.00[YRI][hapmap]
rs16883454	1.00[YRI][hapmap]
rs16883506	0.81[CEU][hapmap]
rs16883549	1.00[CEU][hapmap];0.89[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16883689	1.00[CEU][hapmap];0.84[CHB][hapmap];1.00[YRI][hapmap];0.84[AMR][1000 genomes]
rs16883753	1.00[CEU][hapmap];0.85[CHB][hapmap]
rs1861754	0.81[CEU][hapmap]
rs1861755	1.00[YRI][hapmap]
rs1993207	1.00[CEU][hapmap];0.85[CHB][hapmap];1.00[YRI][hapmap]
rs2045033	1.00[CEU][hapmap];0.80[CHB][hapmap]
rs2111426	0.81[CEU][hapmap]
rs2123489	1.00[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];0.80[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs2131297	0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2167777	0.88[ASN][1000 genomes]
rs2201203	0.81[CEU][hapmap]
rs2353271	1.00[YRI][hapmap]
rs28661390	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28762986	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3922407	0.81[CEU][hapmap];1.00[YRI][hapmap]
rs4363229	1.00[CEU][hapmap];0.85[CHB][hapmap];1.00[YRI][hapmap];0.81[AMR][1000 genomes]
rs5004568	0.81[AMR][1000 genomes]
rs5014673	0.80[ASN][1000 genomes]
rs62514456	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62516467	0.81[AMR][1000 genomes]
rs62516479	0.80[AMR][1000 genomes]
rs6415459	1.00[YRI][hapmap]
rs6986274	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7006962	1.00[CEU][hapmap];0.85[CHB][hapmap]
rs7017899	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7463918	1.00[CEU][hapmap];0.85[CHB][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7824183	1.00[CEU][hapmap];0.85[CHB][hapmap];1.00[YRI][hapmap];0.81[AMR][1000 genomes]
rs7825635	1.00[YRI][hapmap]
rs7826270	0.81[CEU][hapmap];1.00[YRI][hapmap]
rs7832171	1.00[CEU][hapmap];0.85[CHB][hapmap]
rs7835735	0.91[CEU][hapmap]
rs7836340	1.00[CEU][hapmap]
rs7844829	1.00[YRI][hapmap]
rs888254	0.81[CEU][hapmap]
rs929686	0.81[CEU][hapmap]
rs9297476	1.00[CEU][hapmap];0.81[CHB][hapmap]
rs990616	0.81[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533857	chr8:112819659-113801258	Enhancers Bivalent Enhancer Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases
2	nsv1022457	chr8:113071774-113811177	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
3	esv2755868	chr8:113282795-113634842	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	esv2753595	chr8:113283214-114190390	Enhancers Weak transcription Active TSS Strong transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
5	esv2754232	chr8:113294967-113634842	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:113399400-113410600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:113410000-113412400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr8:113410400-113410600	Bivalent Enhancer	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr8:113410400-113410800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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