Variant report

Variant	rs7114261
Chromosome Location	chr11:83827146-83827147
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 131 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:125)

rs_ID	r²[population]
rs1014066	1.00[CEU][hapmap];0.95[CHB][hapmap];0.94[JPT][hapmap];0.94[YRI][hapmap];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10501555	1.00[CEU][hapmap];0.95[CHB][hapmap];0.94[JPT][hapmap];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10736760	1.00[CHB][hapmap];0.88[ASN][1000 genomes]
rs10751104	1.00[CHB][hapmap];0.94[JPT][hapmap];0.98[ASN][1000 genomes]
rs10751105	0.95[CHB][hapmap]
rs10751106	0.90[CHB][hapmap]
rs10751109	0.81[CHB][hapmap]
rs10792712	0.80[CHB][hapmap]
rs10792713	0.90[CHB][hapmap]
rs10792716	0.82[CHB][hapmap]
rs10792717	0.90[CHB][hapmap]
rs10792718	0.90[CHB][hapmap]
rs10792719	0.95[CHB][hapmap];0.94[JPT][hapmap];1.00[YRI][hapmap];0.90[AMR][1000 genomes];0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10792720	0.83[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs10792721	0.92[ASN][1000 genomes]
rs10792722	0.95[CHB][hapmap];0.94[JPT][hapmap];0.85[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs10792723	0.95[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs10792724	0.93[ASN][1000 genomes]
rs10792725	1.00[CHB][hapmap];0.88[ASN][1000 genomes]
rs10792726	0.81[ASN][1000 genomes]
rs10792727	0.95[CHB][hapmap]
rs10792728	0.95[CHB][hapmap]
rs10792731	0.90[CHB][hapmap]
rs10898199	0.90[CHB][hapmap]
rs10898202	0.86[CHB][hapmap];0.82[JPT][hapmap]
rs10898204	0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AMR][1000 genomes];0.82[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10898205	1.00[CHB][hapmap];0.94[JPT][hapmap];0.97[ASN][1000 genomes]
rs10898206	1.00[CHB][hapmap];0.94[JPT][hapmap];0.81[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs10898207	1.00[CHB][hapmap];0.94[JPT][hapmap];0.81[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs11233900	0.82[CHB][hapmap]
rs12363188	0.86[CHB][hapmap];0.83[JPT][hapmap];1.00[YRI][hapmap];0.82[AMR][1000 genomes]
rs1349820	0.90[CHB][hapmap]
rs1377745	0.95[CHB][hapmap];0.85[ASN][1000 genomes]
rs1377746	0.95[CHB][hapmap]
rs1377747	0.95[CHB][hapmap]
rs1377748	0.90[CHB][hapmap]
rs1384751	0.80[CHB][hapmap]
rs1454016	0.91[CHB][hapmap]
rs1454017	0.86[CHB][hapmap]
rs1454018	0.85[ASN][1000 genomes]
rs1454019	1.00[CEU][hapmap];0.95[CHB][hapmap];0.89[YRI][hapmap];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1454026	0.90[CHB][hapmap]
rs1454027	0.90[CHB][hapmap]
rs1551334	0.95[CHB][hapmap]
rs1573570	0.81[CHB][hapmap]
rs1573572	0.95[CHB][hapmap]
rs1573573	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1573574	0.90[CHB][hapmap]
rs1620817	1.00[CHB][hapmap];0.84[YRI][hapmap];0.85[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs1670679	0.85[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs1793037	0.95[CHB][hapmap]
rs1793038	0.95[CHB][hapmap]
rs1793039	0.95[CHB][hapmap]
rs1869472	0.95[CHB][hapmap]
rs1894169	1.00[CHB][hapmap];0.94[JPT][hapmap];0.97[ASN][1000 genomes]
rs1894170	1.00[CHB][hapmap];0.94[JPT][hapmap];0.90[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1894171	0.82[CHB][hapmap]
rs1894172	0.90[CHB][hapmap]
rs1945799	0.95[CHB][hapmap];0.84[JPT][hapmap];0.80[AMR][1000 genomes]
rs1945800	0.90[CHB][hapmap];0.84[JPT][hapmap]
rs1945801	0.81[CHB][hapmap];0.84[JPT][hapmap]
rs1945805	0.80[CHB][hapmap]
rs1945807	0.85[CHB][hapmap];0.82[JPT][hapmap]
rs1945808	0.95[CHB][hapmap];0.94[JPT][hapmap];0.85[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs1945814	0.80[CHB][hapmap]
rs1945819	0.94[ASN][1000 genomes]
rs1945820	0.95[CHB][hapmap];0.94[JPT][hapmap];0.95[ASN][1000 genomes]
rs1945821	0.95[ASN][1000 genomes]
rs1945822	0.95[CHB][hapmap];0.94[JPT][hapmap];0.94[ASN][1000 genomes]
rs1945823	1.00[CHB][hapmap];0.94[JPT][hapmap];0.95[YRI][hapmap];0.92[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs1945824	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.95[YRI][hapmap];0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1945825	1.00[CHB][hapmap];0.94[JPT][hapmap];0.95[ASN][1000 genomes]
rs1945826	0.95[CHB][hapmap];0.94[JPT][hapmap];1.00[YRI][hapmap];0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1945827	0.94[CHB][hapmap];0.94[JPT][hapmap];0.94[ASN][1000 genomes]
rs1945828	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];1.00[YRI][hapmap];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1945832	0.90[CHB][hapmap]
rs1984374	0.82[CHB][hapmap]
rs2000961	1.00[CEU][hapmap];0.95[CHB][hapmap];0.94[YRI][hapmap];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2032401	0.90[CHB][hapmap]
rs2051472	0.90[CHB][hapmap]
rs2105806	0.95[CHB][hapmap];0.94[JPT][hapmap];0.94[ASN][1000 genomes]
rs2156848	0.90[CHB][hapmap]
rs2298830	0.95[CHB][hapmap];0.89[JPT][hapmap]
rs2625510	0.80[CHB][hapmap]
rs3905309	0.82[CHB][hapmap]
rs4547116	0.90[CHB][hapmap]
rs4586191	0.80[CHB][hapmap]
rs4943885	0.80[CHB][hapmap]
rs4943886	0.90[CHB][hapmap]
rs4944460	0.80[CHB][hapmap]
rs4944461	0.90[CHB][hapmap]
rs4944463	0.90[CHB][hapmap]
rs4944464	0.82[CHB][hapmap]
rs4944468	0.90[CHB][hapmap]
rs4944471	0.90[CHB][hapmap]
rs4944472	0.90[CHB][hapmap]
rs6592163	0.90[CHB][hapmap]
rs6592164	0.95[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap];0.90[AMR][1000 genomes];0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6592165	0.95[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs7104249	0.95[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.85[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7108582	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];1.00[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7109671	0.90[CHB][hapmap]
rs7114926	0.82[CHB][hapmap]
rs7123516	0.95[CHB][hapmap];0.94[JPT][hapmap];0.92[ASN][1000 genomes]
rs7123584	0.95[CHB][hapmap];0.94[JPT][hapmap];0.92[ASN][1000 genomes]
rs756196	0.95[ASN][1000 genomes]
rs756197	0.95[CHB][hapmap];0.94[JPT][hapmap];0.95[ASN][1000 genomes]
rs7924503	0.82[CHB][hapmap]
rs7924835	0.81[CHB][hapmap]
rs7925643	0.95[CHB][hapmap];0.93[JPT][hapmap];0.85[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7927039	1.00[CHB][hapmap];0.94[JPT][hapmap];0.96[ASN][1000 genomes]
rs7927619	0.82[CHB][hapmap]
rs7928752	0.80[CHB][hapmap]
rs7929117	0.84[ASN][1000 genomes]
rs7935399	0.86[CHB][hapmap];0.84[JPT][hapmap]
rs7941004	0.82[CEU][hapmap];0.90[CHB][hapmap]
rs7943267	0.95[CHB][hapmap]
rs7948263	0.95[CHB][hapmap];0.90[ASN][1000 genomes]
rs872510	0.95[CHB][hapmap];0.94[JPT][hapmap];0.95[ASN][1000 genomes]
rs872511	0.95[CHB][hapmap];0.94[JPT][hapmap];0.95[ASN][1000 genomes]
rs872512	0.95[CHB][hapmap];0.94[JPT][hapmap];0.95[ASN][1000 genomes]
rs884873	0.95[CHB][hapmap];0.94[JPT][hapmap];0.93[ASN][1000 genomes]
rs970226	0.81[CHB][hapmap]
rs9787893	0.84[ASN][1000 genomes]
rs988322	0.90[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1039924	chr11:83662904-83993497	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv541102	chr11:83662904-83993497	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv898029	chr11:83717887-83939591	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	esv2751034	chr11:83801970-83840272	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	n/a
5	nsv1051279	chr11:83818647-83872815	Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv555609	chr11:83822181-83842498	Weak transcription Enhancers	n/a	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:83816600-83829200	Weak transcription	Brain Angular Gyrus	brain
2	chr11:83826600-83827400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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