Variant report

Variant	rs4363970
Chromosome Location	chr2:142244642-142244643
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs10496884	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs11674506	1.00[CEU][hapmap]
rs11675776	1.00[CEU][hapmap]
rs11685267	1.00[CEU][hapmap]
rs12992656	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs12993733	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs12993821	1.00[CEU][hapmap]
rs12994255	0.88[EUR][1000 genomes]
rs13001306	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs13001716	1.00[CHB][hapmap];0.95[ASN][1000 genomes]
rs13006974	1.00[CEU][hapmap]
rs13009586	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13018345	1.00[CHB][hapmap];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13030953	1.00[CEU][hapmap]
rs13393425	0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1471675	1.00[CEU][hapmap]
rs17548023	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs17552442	1.00[CEU][hapmap]
rs17616060	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs17734546	1.00[CEU][hapmap]
rs17735355	1.00[CEU][hapmap]
rs17735674	1.00[CEU][hapmap]
rs17791242	1.00[CEU][hapmap]
rs17791266	1.00[CEU][hapmap]
rs17792070	1.00[CEU][hapmap]
rs1842932	1.00[CEU][hapmap]
rs2890614	1.00[CEU][hapmap]
rs34050146	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs34470585	0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs34571231	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36057199	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4340448	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4588128	1.00[CEU][hapmap];1.00[CHB][hapmap];0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs60727330	0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6429882	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs66741925	0.88[EUR][1000 genomes]
rs6717454	1.00[CEU][hapmap];0.97[EUR][1000 genomes]
rs6741998	1.00[CEU][hapmap];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6746208	1.00[CEU][hapmap];1.00[CHB][hapmap];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6748629	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs6759190	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73963094	0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7579392	1.00[CEU][hapmap]
rs7585876	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs7592963	1.00[CEU][hapmap]
rs7592987	1.00[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv817518	chr2:141714174-142287302	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv583203	chr2:142055133-142378975	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	esv2759095	chr2:142071391-142245947	Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv875234	chr2:142156180-142254119	Enhancers Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
5	esv2756949	chr2:142196123-142245947	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
6	nsv875240	chr2:142199421-142347455	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	inside rSNPs	n/a
7	nsv875243	chr2:142219033-142259592	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
8	nsv459607	chr2:142226768-142263400	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
9	nsv583207	chr2:142226768-142263400	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:142239400-142256400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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