Variant report

Variant	rs11135356
Chromosome Location	chr5:164631618-164631619
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:33)

rs_ID	r²[population]
rs10078215	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10515891	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11135347	0.80[EUR][1000 genomes]
rs11135353	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11135354	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11135357	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11135360	0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13156646	0.92[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13162946	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs13165528	0.86[AFR][1000 genomes];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1363117	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1421701	0.89[EUR][1000 genomes]
rs1421713	0.89[EUR][1000 genomes]
rs1433004	0.92[CEU][hapmap];0.81[CHB][hapmap];0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs28450493	0.82[EUR][1000 genomes]
rs34405444	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4323250	0.86[EUR][1000 genomes]
rs4362959	0.81[EUR][1000 genomes]
rs4431365	0.86[EUR][1000 genomes]
rs4577712	0.87[EUR][1000 genomes]
rs4868916	0.94[ASN][1000 genomes]
rs4868917	0.93[ASN][1000 genomes]
rs6556809	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6556813	0.87[AFR][1000 genomes];0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6870031	0.89[EUR][1000 genomes]
rs6876275	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6884200	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6895570	0.85[EUR][1000 genomes]
rs7447491	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7701554	0.89[EUR][1000 genomes]
rs7736590	0.88[EUR][1000 genomes]
rs885477	0.89[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs969903	0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv528624	chr5:164319435-164701201	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv1033866	chr5:164419608-164677758	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv1027138	chr5:164563093-164852655	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv537937	chr5:164563093-164852655	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv1028006	chr5:164563293-164852516	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv537938	chr5:164563293-164852516	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv1027103	chr5:164606534-164694498	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:164628600-164633400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr5:164630000-164635800	Weak transcription	Fetal Heart	heart

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