Variant report

Variant	rs1525990
Chromosome Location	chr1:73243049-73243050
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10889968	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10889983	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10889984	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11209988	0.83[EUR][1000 genomes]
rs11209999	0.81[ASN][1000 genomes]
rs11210017	0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11210027	0.86[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11210030	0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11210053	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11589065	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12024784	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12029382	0.83[EUR][1000 genomes]
rs12038578	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12042334	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12047199	0.81[EUR][1000 genomes]
rs12402702	0.94[CEU][hapmap];1.00[JPT][hapmap]
rs12406649	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12749370	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1358040	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1534173	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1998719	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2204499	1.00[CEU][hapmap];0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2243622	0.94[CEU][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2265053	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2841185	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2841187	0.89[YRI][hapmap]
rs4147191	0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4259588	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4294370	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4372200	0.83[CEU][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4424448	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4650145	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4650146	0.81[ASN][1000 genomes]
rs6685232	0.94[CEU][hapmap];1.00[JPT][hapmap]
rs6691430	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7514475	0.81[EUR][1000 genomes]
rs7517246	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7526444	0.83[EUR][1000 genomes]
rs9326106	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv871636	chr1:73048685-73274919	ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv871181	chr1:73084221-73305593	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	esv2757735	chr1:73181612-73307170	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	esv2758941	chr1:73181612-73307170	Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv1013549	chr1:73209040-73408373	Flanking Active TSS Active TSS Enhancers Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 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	chr1:73242400-73243600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr1:73243000-73243400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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