Variant report

Variant	rs1382469
Chromosome Location	chr8:114363347-114363348
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs10096816	0.81[CHB][hapmap];0.82[JPT][hapmap];0.81[YRI][hapmap]
rs10103599	0.81[CHB][hapmap];0.82[JPT][hapmap]
rs10107860	0.81[CHB][hapmap];0.82[JPT][hapmap]
rs10108074	0.81[CHB][hapmap];0.82[CHD][hapmap];0.82[JPT][hapmap]
rs10447963	0.82[JPT][hapmap]
rs10447988	0.80[CHB][hapmap];0.85[JPT][hapmap]
rs10955650	0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs10955654	0.81[CHB][hapmap];0.81[JPT][hapmap]
rs10955655	0.81[CHB][hapmap];0.82[JPT][hapmap]
rs10955656	0.81[CHB][hapmap];0.82[JPT][hapmap]
rs12542594	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs12545118	0.81[CHB][hapmap];0.82[JPT][hapmap];0.81[YRI][hapmap]
rs12547550	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs12548951	0.81[CHB][hapmap];0.82[CHD][hapmap];0.82[JPT][hapmap]
rs12549502	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs12550801	1.00[CEU][hapmap]
rs1402942	0.81[CHB][hapmap];0.82[JPT][hapmap]
rs1402944	0.93[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.98[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.91[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];0.92[YRI][hapmap]
rs1480452	1.00[CEU][hapmap];0.81[GIH][hapmap];0.96[TSI][hapmap]
rs1480459	0.82[CHD][hapmap];0.81[YRI][hapmap]
rs1522059	1.00[ASW][hapmap];1.00[CEU][hapmap];0.95[CHB][hapmap];0.93[CHD][hapmap];1.00[GIH][hapmap];0.94[JPT][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap]
rs1522060	1.00[ASW][hapmap];1.00[CEU][hapmap];0.90[CHB][hapmap];0.93[CHD][hapmap];1.00[GIH][hapmap];0.94[JPT][hapmap];0.95[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.96[TSI][hapmap];1.00[YRI][hapmap]
rs1522061	0.81[CHB][hapmap];0.82[JPT][hapmap];0.81[YRI][hapmap]
rs1551959	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1585720	0.81[CHB][hapmap];0.82[JPT][hapmap]
rs16892637	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];1.00[MKK][hapmap];0.96[TSI][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17609383	1.00[CEU][hapmap];0.90[CHB][hapmap]
rs17840621	0.90[AFR][1000 genomes];0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2127690	0.95[CHB][hapmap];1.00[JPT][hapmap]
rs2177112	0.81[CHB][hapmap];0.82[CHD][hapmap];0.82[JPT][hapmap]
rs2219898	0.95[CHB][hapmap];0.98[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.83[TSI][hapmap]
rs4242552	0.81[CHB][hapmap];0.82[JPT][hapmap];0.81[YRI][hapmap]
rs4320578	0.81[CHB][hapmap];0.82[JPT][hapmap]
rs4333631	0.95[CHB][hapmap];1.00[JPT][hapmap]
rs4370561	0.81[CHB][hapmap];0.82[JPT][hapmap]
rs4403438	0.81[CHB][hapmap];0.82[JPT][hapmap]
rs4433179	0.81[CHB][hapmap];0.82[JPT][hapmap];0.81[YRI][hapmap]
rs4437686	0.81[CHB][hapmap];0.82[CHD][hapmap];0.82[JPT][hapmap];0.81[YRI][hapmap]
rs62519810	0.84[ASN][1000 genomes]
rs6984847	0.81[CHB][hapmap];0.82[JPT][hapmap]
rs6996176	0.81[CHB][hapmap];0.82[JPT][hapmap];0.81[YRI][hapmap]
rs7001577	0.82[CHD][hapmap]
rs7002376	0.81[CHB][hapmap];0.82[JPT][hapmap];0.81[YRI][hapmap]
rs7002915	0.81[CHB][hapmap];0.83[CHD][hapmap]
rs7012271	0.81[CHB][hapmap];0.82[CHD][hapmap];0.82[JPT][hapmap];0.81[YRI][hapmap]
rs720405	0.81[CHB][hapmap];0.82[CHD][hapmap];0.82[JPT][hapmap]
rs720406	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];0.96[TSI][hapmap]
rs7812921	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs7826077	0.81[CHB][hapmap];0.82[JPT][hapmap];0.81[YRI][hapmap]
rs7833144	0.82[JPT][hapmap]
rs9642820	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9643077	0.81[CHB][hapmap];0.81[JPT][hapmap];0.81[YRI][hapmap]
rs9643078	0.82[JPT][hapmap]
rs984990	0.82[JPT][hapmap];0.81[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2754581	chr8:114029421-114419106	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv817379	chr8:114338391-115011632	Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	esv2754463	chr8:114353649-114501547	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:114362200-114363400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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