Variant report

Variant	rs11041792
Chromosome Location	chr11:8212784-8212785
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10743057	0.86[EUR][1000 genomes]
rs10769882	0.82[AMR][1000 genomes]
rs10839994	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10839995	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10839997	0.88[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs11041785	0.85[ASN][1000 genomes]
rs11041788	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11041791	0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12222717	0.89[ASN][1000 genomes]
rs12278538	0.82[ASN][1000 genomes]
rs12786736	0.81[EUR][1000 genomes]
rs12793315	0.84[EUR][1000 genomes]
rs12802958	0.84[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12808387	0.83[ASN][1000 genomes]
rs1569127	0.84[ASN][1000 genomes]
rs1918847	0.84[ASN][1000 genomes]
rs34809738	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs35727940	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3849992	0.81[EUR][1000 genomes]
rs4123670	0.81[EUR][1000 genomes]
rs4123671	0.81[EUR][1000 genomes]
rs4570568	0.84[ASN][1000 genomes]
rs4758048	0.82[EUR][1000 genomes]
rs4758305	0.86[ASN][1000 genomes]
rs4758307	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4758308	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4758309	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4758310	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7112519	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7115706	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7117673	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7122882	0.82[AMR][1000 genomes]
rs7127259	0.89[ASN][1000 genomes]
rs7482621	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7931434	0.86[ASN][1000 genomes]
rs7939157	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7941224	0.88[ASN][1000 genomes]
rs7948836	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7952275	0.84[ASN][1000 genomes]
rs9783292	0.84[EUR][1000 genomes]
rs9783334	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1829170	chr11:8068594-8216369	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
2	nsv428249	chr11:8068594-8216369	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
3	nsv896981	chr11:8152080-8227964	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv1054339	chr11:8153582-8263173	Bivalent Enhancer Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	esv1826805	chr11:8201022-8215751	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	esv1829890	chr11:8201022-8215751	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv553444	chr11:8201125-8215751	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv553445	chr11:8201305-8215853	Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:8202600-8213800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr11:8212000-8213000	Enhancers	Brain Germinal Matrix	brain
3	chr11:8212400-8212800	Bivalent Enhancer	Fetal Stomach	stomach
4	chr11:8212400-8213000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin

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