Variant report

Variant	rs61953357
Chromosome Location	chr13:62161035-62161036
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11616619	0.98[EUR][1000 genomes]
rs11617966	0.98[EUR][1000 genomes]
rs11618197	0.98[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11618840	0.97[EUR][1000 genomes]
rs12583182	0.98[EUR][1000 genomes]
rs12583674	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12584815	0.98[EUR][1000 genomes]
rs12854026	0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12855361	0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12856551	0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12856668	0.96[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12857633	0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12865850	0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12866117	0.89[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12866522	0.96[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12870813	0.98[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12871968	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12873364	0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12877762	0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs17060075	0.82[ASN][1000 genomes]
rs17060076	0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17070255	0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2329308	0.81[ASN][1000 genomes]
rs34157221	0.98[EUR][1000 genomes]
rs34472182	0.98[EUR][1000 genomes]
rs34486297	0.98[EUR][1000 genomes]
rs34572426	0.98[EUR][1000 genomes]
rs34689230	0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs34768890	0.98[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs35278423	0.95[EUR][1000 genomes]
rs35544122	0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs35990992	0.98[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs36115037	0.98[EUR][1000 genomes]
rs4884390	0.98[EUR][1000 genomes]
rs4886343	0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4886344	0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs57749251	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs59756022	0.97[EUR][1000 genomes]
rs60915788	0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs61953379	0.98[EUR][1000 genomes]
rs61955263	0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948661	chr13:61906251-62179649	Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	esv2761266	chr13:61928642-62690828	Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv948810	chr13:62003256-62968196	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	nsv1053698	chr13:62108064-62271909	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
5	nsv900249	chr13:62133250-62218811	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
6	nsv900250	chr13:62147535-62321073	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:62160400-62162000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr13:62161000-62161600	Enhancers	Brain Substantia Nigra	brain

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