Variant report

Variant	rs1147047
Chromosome Location	chr11:104658551-104658552
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 60 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs10128735	0.84[ASN][1000 genomes]
rs10791726	0.82[ASN][1000 genomes]
rs10895725	0.84[EUR][1000 genomes]
rs10895726	0.88[EUR][1000 genomes]
rs10895727	0.88[EUR][1000 genomes]
rs11226478	0.85[EUR][1000 genomes]
rs11226487	0.87[EUR][1000 genomes]
rs11226489	0.90[EUR][1000 genomes]
rs1147027	0.90[EUR][1000 genomes]
rs1147028	0.90[EUR][1000 genomes]
rs1147030	0.90[EUR][1000 genomes]
rs1147035	0.85[ASN][1000 genomes]
rs1147036	0.91[ASN][1000 genomes]
rs1147037	0.91[ASN][1000 genomes]
rs1147040	0.91[ASN][1000 genomes]
rs1147042	0.93[ASN][1000 genomes]
rs1147046	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1147051	0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1200639	0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1200640	0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1200641	0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1200644	0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1200648	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1200649	0.91[ASN][1000 genomes]
rs1200653	0.82[ASN][1000 genomes]
rs1200656	0.91[ASN][1000 genomes]
rs1201819	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12272453	0.84[ASN][1000 genomes]
rs12280706	0.84[ASN][1000 genomes]
rs12788324	0.84[ASN][1000 genomes]
rs1365393	0.82[ASN][1000 genomes]
rs1426550	0.84[ASN][1000 genomes]
rs1426551	0.82[ASN][1000 genomes]
rs1426552	0.84[ASN][1000 genomes]
rs1426553	0.84[ASN][1000 genomes]
rs1834631	0.84[ASN][1000 genomes]
rs1892927	0.84[ASN][1000 genomes]
rs1944539	0.85[EUR][1000 genomes]
rs2052752	0.84[ASN][1000 genomes]
rs2845897	0.91[ASN][1000 genomes]
rs2850820	0.85[EUR][1000 genomes]
rs34185315	0.84[ASN][1000 genomes]
rs34462521	0.84[ASN][1000 genomes]
rs35835077	0.84[ASN][1000 genomes]
rs4466799	0.81[EUR][1000 genomes]
rs4494280	0.84[ASN][1000 genomes]
rs4619123	0.84[ASN][1000 genomes]
rs4755048	0.86[EUR][1000 genomes]
rs4755049	0.85[EUR][1000 genomes]
rs60489722	0.84[ASN][1000 genomes]
rs7122441	0.85[EUR][1000 genomes]
rs7130311	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7925694	0.84[ASN][1000 genomes]
rs7926917	0.85[ASN][1000 genomes]
rs985406	0.85[ASN][1000 genomes]

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	nsv1044271	chr11:104136156-104666252	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv1046098	chr11:104207210-105003661	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
3	nsv1054456	chr11:104358924-104805251	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv531430	chr11:104380924-105194452	Genic enhancers Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
5	nsv1050346	chr11:104548749-104664665	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:104655800-104668600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood

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