Variant report

Variant	rs9325094
Chromosome Location	chr5:147729791-147729792
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 103 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:102)

rs_ID	r²[population]
rs10036053	0.85[EUR][1000 genomes]
rs10037318	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10041283	0.88[CHB][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs10043775	0.88[CHB][hapmap];1.00[JPT][hapmap]
rs10044054	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs10044061	0.89[CHB][hapmap];0.94[JPT][hapmap];0.84[ASN][1000 genomes]
rs10050560	0.84[CEU][hapmap];0.85[EUR][1000 genomes]
rs10057472	0.89[EUR][1000 genomes]
rs10060180	0.86[EUR][1000 genomes]
rs10060753	0.86[CEU][hapmap];0.89[CHB][hapmap];0.88[JPT][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10068216	0.88[CHB][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs10068891	0.90[CEU][hapmap];0.89[EUR][1000 genomes]
rs10072051	0.89[CHB][hapmap];0.94[JPT][hapmap];0.84[ASN][1000 genomes]
rs10072817	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10072958	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10077690	0.85[CEU][hapmap];0.88[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs10476892	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10477374	0.93[EUR][1000 genomes]
rs10477376	0.88[CHB][hapmap];1.00[JPT][hapmap]
rs10515610	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12513547	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs12516267	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12519039	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12521065	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12717971	0.87[EUR][1000 genomes]
rs12717973	0.85[CEU][hapmap];0.88[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs13153619	0.91[EUR][1000 genomes]
rs13157347	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13158948	0.80[AFR][1000 genomes];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13176114	0.89[EUR][1000 genomes]
rs13358385	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1345741	0.82[CEU][hapmap]
rs1363704	0.85[EUR][1000 genomes]
rs1363705	0.87[EUR][1000 genomes]
rs1363707	0.95[CEU][hapmap];0.89[EUR][1000 genomes]
rs1422968	0.87[EUR][1000 genomes]
rs1422970	0.87[EUR][1000 genomes]
rs1422976	0.95[CEU][hapmap]
rs1582519	0.95[CEU][hapmap];0.96[EUR][1000 genomes]
rs17108251	0.88[CHB][hapmap];1.00[JPT][hapmap]
rs17719578	0.89[EUR][1000 genomes]
rs17719662	0.85[EUR][1000 genomes]
rs17719763	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs17719873	0.87[EUR][1000 genomes]
rs17776554	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17776674	0.89[EUR][1000 genomes]
rs1862430	0.89[EUR][1000 genomes]
rs1862431	0.85[EUR][1000 genomes]
rs2161432	0.91[EUR][1000 genomes]
rs2216653	0.91[EUR][1000 genomes]
rs2400509	0.95[CEU][hapmap];0.89[EUR][1000 genomes]
rs2400510	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs28442279	0.89[EUR][1000 genomes]
rs2895761	0.87[EUR][1000 genomes]
rs34001290	0.90[EUR][1000 genomes]
rs34163281	0.89[EUR][1000 genomes]
rs34685718	0.82[ASN][1000 genomes]
rs35006442	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs35700061	0.87[EUR][1000 genomes]
rs35792476	0.89[EUR][1000 genomes]
rs3734120	0.88[CHB][hapmap];0.94[JPT][hapmap]
rs3749689	0.95[CEU][hapmap];0.85[EUR][1000 genomes]
rs3749690	0.95[CEU][hapmap];0.89[EUR][1000 genomes]
rs4705247	0.82[CEU][hapmap]
rs4705248	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4705249	0.95[CEU][hapmap];0.85[EUR][1000 genomes]
rs4705251	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4705252	0.95[CEU][hapmap];0.96[EUR][1000 genomes]
rs6580542	0.89[EUR][1000 genomes]
rs6580544	0.86[EUR][1000 genomes]
rs6580545	0.95[CEU][hapmap];0.86[EUR][1000 genomes]
rs6580546	0.95[CEU][hapmap];0.86[EUR][1000 genomes]
rs6580548	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6860261	0.90[EUR][1000 genomes]
rs6865036	0.95[EUR][1000 genomes]
rs6865972	0.90[EUR][1000 genomes]
rs6866106	0.93[EUR][1000 genomes]
rs6875252	0.89[EUR][1000 genomes]
rs6875795	0.86[EUR][1000 genomes]
rs6876308	0.89[EUR][1000 genomes]
rs6876982	1.00[CEU][hapmap];0.83[CHB][hapmap];0.94[JPT][hapmap];0.94[YRI][hapmap];0.87[AFR][1000 genomes];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6882932	0.88[EUR][1000 genomes]
rs6884076	0.85[CHB][hapmap];0.88[JPT][hapmap]
rs6886203	0.85[EUR][1000 genomes]
rs6891724	0.93[EUR][1000 genomes]
rs6892647	0.95[CEU][hapmap];0.86[EUR][1000 genomes]
rs6893378	0.90[EUR][1000 genomes]
rs6894032	0.91[EUR][1000 genomes]
rs7712350	0.89[EUR][1000 genomes]
rs7713986	0.89[EUR][1000 genomes]
rs7716578	0.93[EUR][1000 genomes]
rs7722458	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7729309	0.95[CEU][hapmap];0.96[EUR][1000 genomes]
rs7730707	0.86[EUR][1000 genomes]
rs7731526	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7734458	0.95[CEU][hapmap];0.89[EUR][1000 genomes]
rs7736728	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9325095	0.88[CHB][hapmap];1.00[JPT][hapmap]
rs9325097	0.87[CHB][hapmap];0.93[JPT][hapmap]
rs9325098	0.88[CHB][hapmap];0.94[JPT][hapmap]
rs9784645	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs999741	0.91[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv883015	chr5:147404281-147751035	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:147709400-147749200	Weak transcription	Psoas Muscle	Psoas
2	chr5:147714800-147731200	Weak transcription	Pancreas	Pancrea
3	chr5:147723600-147751600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr5:147727600-147732200	Weak transcription	Fetal Brain Female	brain
5	chr5:147729000-147730200	Strong transcription	Left Ventricle	heart
6	chr5:147729200-147762200	Weak transcription	Aorta	Aorta

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