Variant report

Variant	rs7126806
Chromosome Location	chr11:23732511-23732512
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10458857	1.00[ASN][1000 genomes]
rs10741995	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10741996	0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10767108	1.00[ASN][1000 genomes]
rs10767112	0.85[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10834182	0.84[AMR][1000 genomes]
rs10834184	1.00[ASN][1000 genomes]
rs11027434	0.86[EUR][1000 genomes]
rs11027435	0.86[EUR][1000 genomes]
rs11027436	0.86[EUR][1000 genomes]
rs11027437	0.86[EUR][1000 genomes]
rs11027438	0.86[EUR][1000 genomes]
rs11027440	0.86[EUR][1000 genomes]
rs11027446	1.00[EUR][1000 genomes]
rs11027447	1.00[ASN][1000 genomes]
rs11027453	0.94[AMR][1000 genomes]
rs12269913	0.86[EUR][1000 genomes]
rs12274900	0.86[EUR][1000 genomes]
rs12277987	1.00[EUR][1000 genomes]
rs12280993	0.86[EUR][1000 genomes]
rs12282955	0.86[EUR][1000 genomes]
rs12283754	0.86[EUR][1000 genomes]
rs12288125	0.86[EUR][1000 genomes]
rs12289552	0.86[EUR][1000 genomes]
rs12293059	1.00[EUR][1000 genomes]
rs4274196	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4344483	0.82[AMR][1000 genomes]
rs4562830	1.00[ASN][1000 genomes]
rs4923123	0.88[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4923124	0.88[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6483985	1.00[ASN][1000 genomes]
rs7104997	0.87[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7108807	0.88[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7118760	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7119105	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73435840	0.86[EUR][1000 genomes]
rs7933415	1.00[ASN][1000 genomes]
rs7943495	1.00[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	nsv553757	chr11:23564329-23896729	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv897062	chr11:23687928-24031627	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv916840	chr11:23710275-24064119	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	esv1816999	chr11:23723766-23750675	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv897063	chr11:23723766-23940407	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 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	chr11:23732400-23733600	Weak transcription	iPS-20b Cell Line	embryonic stem cell

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