Variant report

Variant	rs2681724
Chromosome Location	chr14:72826546-72826547
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10136263	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10141305	0.83[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs10149207	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1072165	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11620677	0.81[EUR][1000 genomes]
rs1356842	0.86[EUR][1000 genomes]
rs1996661	0.86[EUR][1000 genomes]
rs2090736	0.86[EUR][1000 genomes]
rs2139596	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2190509	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2222311	0.86[EUR][1000 genomes]
rs2239246	0.85[EUR][1000 genomes]
rs2529458	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2529459	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2529465	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2529474	0.84[EUR][1000 genomes]
rs2529476	0.86[EUR][1000 genomes]
rs2681729	0.81[EUR][1000 genomes]
rs2681732	0.94[EUR][1000 genomes]
rs2681738	0.81[EUR][1000 genomes]
rs2681739	0.86[EUR][1000 genomes]
rs2681740	0.83[EUR][1000 genomes]
rs2681750	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2681756	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2681758	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2681760	0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2681763	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2681770	0.84[EUR][1000 genomes]
rs765221	0.84[EUR][1000 genomes]
rs769148	0.87[ASN][1000 genomes]
rs847325	0.87[ASN][1000 genomes]
rs847328	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs847330	0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs847331	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs847334	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs847349	0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530794	chr14:72113818-73034008	Enhancers Bivalent/Poised TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
2	nsv948800	chr14:72462557-73150701	Enhancers Bivalent Enhancer Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 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	chr14:72825200-72828000	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr14:72825200-72829000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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