Variant report

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10136808	0.99[ASN][1000 genomes]
rs10137909	0.95[ASN][1000 genomes]
rs10138176	0.90[CHB][hapmap];0.95[JPT][hapmap];0.95[ASN][1000 genomes]
rs11158926	0.96[CEU][hapmap];0.80[EUR][1000 genomes]
rs11623548	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs11623588	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs12590831	0.95[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs1476745	0.92[CEU][hapmap];0.80[EUR][1000 genomes]
rs17768361	0.92[CEU][hapmap];0.80[EUR][1000 genomes]
rs1978225	0.95[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs1978227	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs2010848	0.95[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs2190873	0.82[CHB][hapmap]
rs2238284	0.86[CHB][hapmap];0.87[JPT][hapmap]
rs2283424	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs2283426	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs2332704	0.94[ASN][1000 genomes]
rs36332	0.81[CHB][hapmap];0.87[JPT][hapmap]
rs3825716	0.91[CHB][hapmap];0.91[JPT][hapmap];0.92[ASN][1000 genomes]
rs4569194	0.99[ASN][1000 genomes]
rs4902964	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs7155855	1.00[CHB][hapmap];0.95[JPT][hapmap];0.92[ASN][1000 genomes]
rs7161596	0.84[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	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

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:72456400-72457200	Weak transcription	Left Ventricle	heart
2	chr14:72456800-72457200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr14:72456800-72457200	Enhancers	Placenta	Placenta
4	chr14:72456800-72457600	Enhancers	Fetal Muscle Leg	muscle
5	chr14:72457000-72457400	Enhancers	Right Ventricle	heart
6	chr14:72457000-72460200	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr14:72457000-72461200	Weak transcription	Fetal Heart	heart

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