Variant report

Variant	rs2135143
Chromosome Location	chr1:75695380-75695381
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10493564	0.89[ASN][1000 genomes]
rs10493565	0.89[ASN][1000 genomes]
rs10493566	0.89[ASN][1000 genomes]
rs10782715	0.89[ASN][1000 genomes]
rs11162847	0.89[ASN][1000 genomes]
rs11162849	0.89[ASN][1000 genomes]
rs11162856	0.89[ASN][1000 genomes]
rs11162870	0.89[ASN][1000 genomes]
rs11162873	0.89[ASN][1000 genomes]
rs11162878	0.89[ASN][1000 genomes]
rs11162880	0.89[ASN][1000 genomes]
rs12095168	0.89[ASN][1000 genomes]
rs12562352	0.89[ASN][1000 genomes]
rs12568950	0.89[ASN][1000 genomes]
rs12568990	0.89[ASN][1000 genomes]
rs1335735	0.89[ASN][1000 genomes]
rs1415461	0.89[ASN][1000 genomes]
rs1505260	0.89[ASN][1000 genomes]
rs1505261	0.89[ASN][1000 genomes]
rs1505262	0.89[ASN][1000 genomes]
rs1505263	0.89[ASN][1000 genomes]
rs17096462	0.89[ASN][1000 genomes]
rs2221459	0.89[ASN][1000 genomes]
rs34755141	0.89[ASN][1000 genomes]
rs4369182	0.89[ASN][1000 genomes]
rs5006253	0.89[ASN][1000 genomes]
rs57612788	0.89[ASN][1000 genomes]
rs587346	0.89[ASN][1000 genomes]
rs587787	0.89[ASN][1000 genomes]
rs588098	0.89[ASN][1000 genomes]
rs596098	0.89[ASN][1000 genomes]
rs598609	0.89[ASN][1000 genomes]
rs60198223	0.89[ASN][1000 genomes]
rs611309	0.89[ASN][1000 genomes]
rs616827	0.96[ASN][1000 genomes]
rs619193	0.89[ASN][1000 genomes]
rs637660	0.89[ASN][1000 genomes]
rs638302	0.89[ASN][1000 genomes]
rs645513	0.82[ASN][1000 genomes]
rs647924	0.89[ASN][1000 genomes]
rs648363	0.89[ASN][1000 genomes]
rs649352	0.89[ASN][1000 genomes]
rs665575	0.89[ASN][1000 genomes]
rs666397	0.89[ASN][1000 genomes]
rs667887	0.89[ASN][1000 genomes]
rs669806	0.89[ASN][1000 genomes]
rs681866	0.82[ASN][1000 genomes]
rs7544408	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs976048	0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv871743	chr1:75235082-75714554	Bivalent Enhancer Strong transcription Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	esv3368999	chr1:75524762-75933220	Bivalent/Poised TSS Strong transcription Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:75676400-75700400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr1:75678800-75705400	Weak transcription	Fetal Brain Female	brain
3	chr1:75685200-75700200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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