Variant report

Variant	rs2511277
Chromosome Location	chr11:71122151-71122152
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs1044535	0.83[AMR][1000 genomes]
rs10898117	1.00[CHB][hapmap];0.85[YRI][hapmap];0.80[AFR][1000 genomes];0.93[AMR][1000 genomes]
rs11233555	1.00[CEU][hapmap]
rs11233606	0.89[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs11608138	0.87[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs1616994	0.97[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1623080	0.92[AMR][1000 genomes]
rs1790325	0.81[AMR][1000 genomes]
rs1790326	0.85[AMR][1000 genomes]
rs1790327	0.83[AMR][1000 genomes]
rs1790329	0.86[AMR][1000 genomes]
rs1790334	0.80[AMR][1000 genomes]
rs1790336	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1790337	1.00[CHB][hapmap];0.89[JPT][hapmap];0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs1790347	0.86[AMR][1000 genomes]
rs1790348	0.83[AMR][1000 genomes]
rs1790354	0.80[AFR][1000 genomes];0.93[AMR][1000 genomes]
rs1790355	0.80[AFR][1000 genomes];0.93[AMR][1000 genomes]
rs1790356	0.80[AFR][1000 genomes];0.93[AMR][1000 genomes]
rs1790357	0.89[AMR][1000 genomes]
rs1790361	0.91[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1790366	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap]
rs1790374	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1792238	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1792243	0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1792265	0.81[AMR][1000 genomes]
rs1792268	0.81[AMR][1000 genomes]
rs1792270	0.86[AMR][1000 genomes]
rs1792271	0.86[AMR][1000 genomes]
rs1792272	0.83[AMR][1000 genomes]
rs1792273	0.83[AMR][1000 genomes]
rs1792274	0.86[AMR][1000 genomes]
rs1792275	0.83[AMR][1000 genomes]
rs1792276	0.82[AMR][1000 genomes]
rs1792279	0.93[AMR][1000 genomes]
rs1792285	0.81[AFR][1000 genomes];0.93[AMR][1000 genomes]
rs1792322	0.91[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs1792326	1.00[YRI][hapmap];0.94[AFR][1000 genomes]
rs1792327	1.00[YRI][hapmap]
rs2511279	0.83[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2851693	0.80[AMR][1000 genomes]
rs7110053	0.89[AFR][1000 genomes];0.93[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs7110316	0.81[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs7124675	0.89[AFR][1000 genomes];0.93[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs760241	0.86[AMR][1000 genomes]
rs949177	0.82[AMR][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	nsv1048123	chr11:70795222-71231382	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	21 gene(s)	inside rSNPs	diseases
2	nsv832202	chr11:71088949-71131368	Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv526973	chr11:71088949-71215880	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
4	nsv897897	chr11:71088949-71217571	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
5	nsv530623	chr11:71088949-72020418	Enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	134 gene(s)	inside rSNPs	diseases
6	nsv897898	chr11:71103143-71211654	Weak transcription ZNF genes & repeats Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
7	nsv519224	chr11:71108341-71215880	Strong transcription Flanking Bivalent TSS/Enh Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
8	esv3345939	chr11:71119404-71123802	Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

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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