Variant report

Variant	rs1036649
Chromosome Location	chr2:189084878-189084879
allele	A/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:38)

rs_ID	r²[population]
rs10175259	0.85[ASN][1000 genomes]
rs10180222	0.87[ASN][1000 genomes]
rs10804020	0.88[JPT][hapmap]
rs10931343	0.98[ASN][1000 genomes]
rs10931344	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11900558	0.98[ASN][1000 genomes]
rs12464904	0.82[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs12613615	0.81[ASN][1000 genomes]
rs12619361	0.87[ASN][1000 genomes]
rs12624002	0.82[JPT][hapmap]
rs12693487	0.98[ASN][1000 genomes]
rs12693489	0.81[ASN][1000 genomes]
rs13008931	0.90[CHB][hapmap];0.88[JPT][hapmap];0.81[YRI][hapmap];0.81[ASN][1000 genomes]
rs1898986	0.95[ASN][1000 genomes]
rs4402719	0.84[ASN][1000 genomes]
rs4426503	0.81[ASN][1000 genomes]
rs4500907	0.98[ASN][1000 genomes]
rs4516391	0.90[CHB][hapmap];0.88[JPT][hapmap];0.86[YRI][hapmap]
rs4591312	0.81[ASN][1000 genomes]
rs4610010	0.81[ASN][1000 genomes]
rs4641903	0.98[ASN][1000 genomes]
rs4667215	0.81[ASN][1000 genomes]
rs6434269	0.95[CHB][hapmap];0.88[JPT][hapmap];0.82[ASN][1000 genomes]
rs6711822	0.95[ASN][1000 genomes]
rs6712056	0.81[ASN][1000 genomes]
rs6719273	0.98[ASN][1000 genomes]
rs6744150	0.98[ASN][1000 genomes]
rs6744629	0.90[CHB][hapmap];0.88[JPT][hapmap];0.86[YRI][hapmap];0.80[ASN][1000 genomes]
rs7425596	0.81[ASN][1000 genomes]
rs7566619	0.88[JPT][hapmap]
rs7574262	0.88[JPT][hapmap]
rs7585703	0.95[CHB][hapmap];0.88[JPT][hapmap];0.84[ASN][1000 genomes]
rs7586390	0.88[JPT][hapmap]
rs7593546	0.90[CHB][hapmap];0.88[JPT][hapmap];0.85[YRI][hapmap];0.81[ASN][1000 genomes]
rs7598279	0.84[ASN][1000 genomes]
rs7598785	0.98[ASN][1000 genomes]
rs7599516	0.84[ASN][1000 genomes]
rs893745	0.95[CHB][hapmap];1.00[JPT][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	nsv1010394	chr2:188994398-189284092	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases
2	nsv998395	chr2:189018246-189284092	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
3	nsv431879	chr2:189079494-189118494	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr2:189084000-189085200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr2:189084400-189085000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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