Variant report

Variant	rs11052414
Chromosome Location	chr12:33207116-33207117
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10459093	0.87[EUR][1000 genomes]
rs10844421	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10844422	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10844430	0.81[ASN][1000 genomes]
rs10844433	0.94[CHB][hapmap];0.83[JPT][hapmap];0.80[ASN][1000 genomes]
rs11052370	0.82[ASN][1000 genomes]
rs11052371	0.82[ASN][1000 genomes]
rs11052375	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11052376	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11052377	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11052378	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11052379	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11052380	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11052391	0.89[AMR][1000 genomes]
rs11052394	0.81[ASN][1000 genomes]
rs11052402	0.80[ASN][1000 genomes]
rs11052407	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12227331	0.81[ASN][1000 genomes]
rs12231642	0.81[ASN][1000 genomes]
rs12231850	1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12578228	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12579660	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12581266	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12812935	0.82[ASN][1000 genomes]
rs1500053	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1500065	0.94[CHB][hapmap];0.84[JPT][hapmap];0.80[ASN][1000 genomes]
rs1500071	0.82[ASN][1000 genomes]
rs1500077	0.87[EUR][1000 genomes]
rs1811678	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1846634	0.80[ASN][1000 genomes]
rs2133675	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs36061762	0.80[ASN][1000 genomes]
rs67487821	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs72640188	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7299289	0.81[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	nsv530421	chr12:32825335-33465991	Strong transcription Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
2	nsv832367	chr12:33063644-33298967	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv1039909	chr12:33132909-33244419	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv1053849	chr12:33132909-33279169	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv1044931	chr12:33179957-33307362	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	2 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	chr12:33201600-33209200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell

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