Variant report

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10489553	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10889845	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10889846	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10889847	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11209508	0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12023616	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12023624	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12023834	0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12041861	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12044761	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12047807	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12048889	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12048977	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1582204	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4440810	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4486403	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72938920	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7512342	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7515290	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7525565	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7525668	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs800930	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs800931	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949691	chr1:69749722-70302201	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	esv3384194	chr1:69885024-70275430	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv830126	chr1:70014879-70167979	Weak transcription Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	esv2764189	chr1:70111889-70137513	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:70135200-70137200	Weak transcription	NH-A	brain
2	chr1:70135400-70137000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr1:70136000-70137000	Weak transcription	Brain Anterior Caudate	brain
4	chr1:70136000-70137600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr1:70136200-70137200	Enhancers	Fetal Brain Male	brain

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