Variant report

Variant	rs11487852
Chromosome Location	chr1:222704639-222704640
allele	A/G
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:37)

rs_ID	r²[population]
rs11487812	0.96[EUR][1000 genomes]
rs12042675	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1487525	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17163152	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17163175	0.98[EUR][1000 genomes]
rs17163177	0.81[ASN][1000 genomes]
rs1890069	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2129637	0.97[EUR][1000 genomes]
rs34130633	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs34136100	0.96[EUR][1000 genomes]
rs34256442	0.98[EUR][1000 genomes]
rs34341350	0.97[EUR][1000 genomes]
rs34784304	0.90[EUR][1000 genomes]
rs34916216	0.95[EUR][1000 genomes]
rs35170234	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs35713066	0.96[EUR][1000 genomes]
rs35759615	0.97[EUR][1000 genomes]
rs3828079	0.97[EUR][1000 genomes]
rs4846369	0.98[EUR][1000 genomes]
rs4846370	0.98[EUR][1000 genomes]
rs4846371	0.98[EUR][1000 genomes]
rs4846373	0.98[EUR][1000 genomes]
rs4846374	0.97[EUR][1000 genomes]
rs4846375	0.97[EUR][1000 genomes]
rs4846376	0.97[EUR][1000 genomes]
rs4846377	0.97[EUR][1000 genomes]
rs4846378	0.97[EUR][1000 genomes]
rs4846381	0.97[EUR][1000 genomes]
rs4846760	0.98[EUR][1000 genomes]
rs4846761	0.98[EUR][1000 genomes]
rs4846763	0.98[EUR][1000 genomes]
rs61825499	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs61825500	0.97[EUR][1000 genomes]
rs61825501	0.97[EUR][1000 genomes]
rs61825516	0.97[EUR][1000 genomes]
rs67978793	0.96[EUR][1000 genomes]
rs958933	0.98[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv873203	chr1:222332906-222775000	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
2	nsv999185	chr1:222500725-223278032	Strong transcription Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
3	nsv535304	chr1:222500725-223278032	Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 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	chr1:222704400-222713000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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