Variant report

Variant	rs35057973
Chromosome Location	chr8:20966267-20966268
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs12543521	1.00[ASN][1000 genomes]
rs13252980	1.00[ASN][1000 genomes]
rs13274991	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13276572	1.00[ASN][1000 genomes]
rs17093549	1.00[ASN][1000 genomes]
rs17093555	1.00[ASN][1000 genomes]
rs17093564	1.00[ASN][1000 genomes]
rs17093578	1.00[ASN][1000 genomes]
rs17423926	1.00[ASN][1000 genomes]
rs17495702	1.00[ASN][1000 genomes]
rs17495757	1.00[ASN][1000 genomes]
rs17495792	1.00[ASN][1000 genomes]
rs17495841	1.00[ASN][1000 genomes]
rs1841509	1.00[ASN][1000 genomes]
rs34224528	1.00[ASN][1000 genomes]
rs34757817	1.00[ASN][1000 genomes]
rs35248934	1.00[ASN][1000 genomes]
rs35325460	1.00[ASN][1000 genomes]
rs35549782	1.00[ASN][1000 genomes]
rs35627243	1.00[ASN][1000 genomes]
rs35698958	1.00[ASN][1000 genomes]
rs35816769	1.00[ASN][1000 genomes]
rs35888205	1.00[ASN][1000 genomes]
rs36082431	1.00[ASN][1000 genomes]
rs36096496	1.00[ASN][1000 genomes]
rs4582551	1.00[ASN][1000 genomes]
rs66823428	1.00[ASN][1000 genomes]
rs67413955	1.00[ASN][1000 genomes]
rs67922235	1.00[ASN][1000 genomes]
rs71513804	1.00[ASN][1000 genomes]
rs71513806	1.00[ASN][1000 genomes]
rs71513807	1.00[ASN][1000 genomes]
rs71513808	1.00[ASN][1000 genomes]
rs73623456	1.00[ASN][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	nsv1032450	chr8:20514995-21033577	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv539524	chr8:20514995-21033577	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	nsv1034265	chr8:20742935-21152545	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
4	nsv539528	chr8:20742935-21152545	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
5	nsv831260	chr8:20907266-21097125	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv469878	chr8:20955260-21128307	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv482339	chr8:20955260-21128307	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region 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	chr8:20965200-20966400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr8:20966200-20966600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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