Variant report

Variant	rs7103649
Chromosome Location	chr11:83754364-83754365
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 100 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:89)

rs_ID	r²[population]
rs10501553	0.97[ASN][1000 genomes]
rs10792705	0.94[CHB][hapmap];1.00[JPT][hapmap]
rs10792707	0.94[CHB][hapmap];1.00[JPT][hapmap]
rs10792710	0.94[CHB][hapmap];1.00[JPT][hapmap]
rs10792711	0.97[ASN][1000 genomes]
rs10792712	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs10792713	0.89[CHB][hapmap]
rs10792716	0.90[CHB][hapmap];0.80[JPT][hapmap]
rs10792717	0.89[CHB][hapmap]
rs10792718	0.89[CHB][hapmap]
rs10898192	0.94[CHB][hapmap];1.00[JPT][hapmap]
rs10898194	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10898199	0.89[CHB][hapmap]
rs10898202	0.85[CHB][hapmap]
rs10898205	0.80[CHB][hapmap]
rs10898207	0.80[CHB][hapmap]
rs11233881	0.90[ASN][1000 genomes]
rs11233890	0.94[ASN][1000 genomes]
rs11233900	0.90[CHB][hapmap];0.86[JPT][hapmap]
rs12285610	1.00[CEU][hapmap];0.86[JPT][hapmap];0.88[YRI][hapmap];0.95[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs12363188	0.85[CHB][hapmap]
rs12574301	0.94[CHB][hapmap];0.91[JPT][hapmap]
rs12577433	0.90[CHB][hapmap];0.80[JPT][hapmap]
rs12806160	0.85[AFR][1000 genomes];0.86[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs1384751	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1483384	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs1540188	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1573570	0.89[CHB][hapmap]
rs1573574	0.89[CHB][hapmap]
rs1601095	0.94[CHB][hapmap];1.00[JPT][hapmap]
rs1894171	0.90[CHB][hapmap];0.80[JPT][hapmap]
rs1894172	0.89[CHB][hapmap]
rs1945799	0.84[CHB][hapmap]
rs1945800	0.89[CHB][hapmap]
rs1945801	0.89[CHB][hapmap]
rs1945802	0.85[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs1945803	0.85[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs1945804	0.82[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs1945805	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs1945807	0.85[CHB][hapmap]
rs1945809	0.89[ASN][1000 genomes]
rs1945811	0.85[ASN][1000 genomes]
rs1945812	0.83[ASN][1000 genomes]
rs1945813	0.93[ASN][1000 genomes]
rs1945814	1.00[CHB][hapmap];0.93[JPT][hapmap];0.91[ASN][1000 genomes]
rs1945815	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs1945816	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1945817	0.94[ASN][1000 genomes]
rs1945828	0.80[CHB][hapmap]
rs1945832	0.89[CHB][hapmap]
rs1984374	0.90[CHB][hapmap];0.80[JPT][hapmap]
rs2032401	0.89[CHB][hapmap]
rs2051472	0.89[CHB][hapmap]
rs2298830	0.84[CHB][hapmap]
rs2514168	0.89[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs2625510	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2625514	0.94[CHB][hapmap];1.00[JPT][hapmap]
rs2625518	0.94[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs2853022	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2853023	0.93[CHB][hapmap];1.00[JPT][hapmap]
rs2853024	0.84[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs34555244	0.95[ASN][1000 genomes]
rs3905309	0.90[CHB][hapmap];0.80[JPT][hapmap]
rs4373957	0.90[AFR][1000 genomes];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4373958	0.83[AFR][1000 genomes]
rs4421763	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4528354	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4586191	1.00[CHB][hapmap];0.93[JPT][hapmap];0.83[YRI][hapmap];0.93[ASN][1000 genomes]
rs4943885	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4943886	0.89[CHB][hapmap]
rs4944459	0.88[AFR][1000 genomes];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4944460	1.00[CHB][hapmap];0.93[JPT][hapmap];0.93[ASN][1000 genomes]
rs4944461	0.89[CHB][hapmap]
rs4944463	0.89[CHB][hapmap]
rs4944464	0.90[CHB][hapmap]
rs6592163	0.89[CHB][hapmap]
rs7108582	0.80[CHB][hapmap]
rs7109671	0.89[CHB][hapmap]
rs7114926	0.90[CHB][hapmap];0.80[JPT][hapmap]
rs7924476	0.88[CHB][hapmap]
rs7924503	0.90[CHB][hapmap]
rs7924835	0.90[CHB][hapmap];0.80[JPT][hapmap]
rs7927039	0.80[CHB][hapmap]
rs7927619	0.90[CHB][hapmap];0.80[JPT][hapmap]
rs7928752	1.00[CHB][hapmap];0.93[JPT][hapmap];0.93[ASN][1000 genomes]
rs7929774	0.87[CHB][hapmap]
rs7935399	0.85[CHB][hapmap]
rs7952399	0.83[CHB][hapmap];0.83[JPT][hapmap]
rs963146	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv898025	chr11:83658909-83796678	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
2	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
3	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
4	nsv898026	chr11:83685801-83789540	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a
5	esv1814410	chr11:83696133-83775326	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a
6	esv1809938	chr11:83716145-83789540	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a
7	nsv898027	chr11:83717887-83798485	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a
8	nsv898028	chr11:83717887-83817360	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	n/a
9	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
10	nsv898030	chr11:83730570-83789540	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a
11	esv1806027	chr11:83740599-83775326	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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