Variant report

Variant	rs11943896
Chromosome Location	chr4:98101079-98101080
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:44)

rs_ID	r²[population]
rs10009327	0.88[ASN][1000 genomes]
rs10021132	0.96[ASN][1000 genomes]
rs10029947	0.96[ASN][1000 genomes]
rs10031646	0.88[ASN][1000 genomes]
rs10452174	0.89[ASN][1000 genomes]
rs11097553	0.96[ASN][1000 genomes]
rs11936576	0.97[ASN][1000 genomes]
rs11941787	0.96[ASN][1000 genomes]
rs13112292	0.86[ASN][1000 genomes]
rs13134423	0.96[ASN][1000 genomes]
rs1462763	0.96[ASN][1000 genomes]
rs28378393	0.96[ASN][1000 genomes]
rs34817974	0.96[ASN][1000 genomes]
rs4075059	0.86[ASN][1000 genomes]
rs4235428	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4295269	0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4295270	0.95[ASN][1000 genomes]
rs4301123	0.86[ASN][1000 genomes]
rs4305515	0.96[ASN][1000 genomes]
rs4317212	0.99[ASN][1000 genomes]
rs4359906	0.96[ASN][1000 genomes]
rs4407512	0.97[ASN][1000 genomes]
rs4443291	0.97[ASN][1000 genomes]
rs4538486	0.96[ASN][1000 genomes]
rs4540053	0.97[ASN][1000 genomes]
rs4599417	0.84[ASN][1000 genomes]
rs4643817	0.97[ASN][1000 genomes]
rs4699304	0.82[ASN][1000 genomes]
rs4699307	0.97[ASN][1000 genomes]
rs4699308	0.97[ASN][1000 genomes]
rs58721082	0.98[ASN][1000 genomes]
rs6532664	0.96[ASN][1000 genomes]
rs6825931	0.99[ASN][1000 genomes]
rs6835997	0.83[ASN][1000 genomes]
rs6855655	0.84[ASN][1000 genomes]
rs6858100	0.99[ASN][1000 genomes]
rs7660918	0.88[ASN][1000 genomes]
rs7670330	0.83[ASN][1000 genomes]
rs7680378	0.84[ASN][1000 genomes]
rs7684189	0.96[ASN][1000 genomes]
rs9784400	0.97[ASN][1000 genomes]
rs9917982	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9994700	0.86[ASN][1000 genomes]
rs9997275	0.96[ASN][1000 genomes]

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	nsv879640	chr4:97711707-98697586	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1002766	chr4:98006688-98128416	Enhancers ZNF genes & repeats Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv537192	chr4:98006688-98128416	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr4:98100400-98101400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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