Variant report

Variant	rs12510298
Chromosome Location	chr4:96736478-96736479
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:40)

rs_ID	r²[population]
rs10000897	0.91[ASN][1000 genomes]
rs10008305	0.93[ASN][1000 genomes]
rs10011321	0.90[ASN][1000 genomes]
rs10019264	0.94[ASN][1000 genomes]
rs10026739	0.88[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];0.84[ASN][1000 genomes]
rs1006643	1.00[CHB][hapmap];0.81[CHD][hapmap];0.90[JPT][hapmap];0.91[ASN][1000 genomes]
rs10212672	0.91[ASN][1000 genomes]
rs10212751	0.93[ASN][1000 genomes]
rs10212823	0.93[ASN][1000 genomes]
rs1076860	1.00[CHB][hapmap];0.81[CHD][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs11097486	0.91[ASN][1000 genomes]
rs12506801	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13104815	0.91[ASN][1000 genomes]
rs13106992	0.91[ASN][1000 genomes]
rs13107501	0.91[ASN][1000 genomes]
rs13114782	0.91[ASN][1000 genomes]
rs13115178	0.91[ASN][1000 genomes]
rs1369982	0.91[ASN][1000 genomes]
rs1436535	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1436539	0.91[ASN][1000 genomes]
rs1436540	0.91[ASN][1000 genomes]
rs1436552	0.97[ASN][1000 genomes]
rs1821736	0.91[ASN][1000 genomes]
rs1821737	0.88[CEU][hapmap];0.82[CHB][hapmap];0.81[JPT][hapmap]
rs1836898	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1836899	0.94[ASN][1000 genomes]
rs2014345	0.82[CEU][hapmap];0.83[JPT][hapmap]
rs4699472	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6532577	0.97[ASN][1000 genomes]
rs6821954	0.91[ASN][1000 genomes]
rs6840758	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6842353	0.93[ASN][1000 genomes]
rs6842388	0.88[ASN][1000 genomes]
rs6842436	0.93[ASN][1000 genomes]
rs6848398	0.91[ASN][1000 genomes]
rs6848743	0.91[ASN][1000 genomes]
rs7659447	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs920155	0.91[ASN][1000 genomes]
rs920157	0.93[ASN][1000 genomes]
rs9998027	0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830012	chr4:96547783-96746163	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv997304	chr4:96575198-96861349	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv1010830	chr4:96607025-96862878	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv537191	chr4:96607025-96862878	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	nsv594915	chr4:96628653-97086618	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
6	nsv428767	chr4:96676384-96831793	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	nsv437405	chr4:96734419-96747103	Enhancers	n/a	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	chr4:96735800-96737400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr4:96736200-96737200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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