Variant report

Variant	rs11031813
Chromosome Location	chr11:32505523-32505524
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10219285	0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11031799	0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11031800	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11031801	0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12271863	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12272661	1.00[ASN][1000 genomes]
rs12276814	0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12277550	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12282084	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12789194	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12789525	0.82[EUR][1000 genomes]
rs12790633	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12794418	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12805730	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12808723	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17748371	1.00[ASN][1000 genomes]
rs35128594	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35245711	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7113208	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7115617	0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7118228	0.85[EUR][1000 genomes]
rs71466594	1.00[ASN][1000 genomes]
rs9300011	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9300012	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9300013	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9651595	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832108	chr11:32395937-32560583	Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 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	chr11:32500800-32510200	Weak transcription	Right Atrium	heart

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