Variant report

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs12633748	0.80[ASN][1000 genomes]
rs12635791	0.80[ASN][1000 genomes]
rs1495887	0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1495890	0.83[ASN][1000 genomes]
rs1603323	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs34120884	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35397503	0.83[ASN][1000 genomes]
rs35706703	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58704257	0.84[ASN][1000 genomes]
rs59095544	0.91[ASN][1000 genomes]
rs59557840	0.84[ASN][1000 genomes]
rs61272271	0.80[ASN][1000 genomes]
rs6783564	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72920670	0.84[ASN][1000 genomes]
rs72920690	0.91[ASN][1000 genomes]
rs73144207	0.83[ASN][1000 genomes]
rs7634263	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7636445	0.82[AFR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9814295	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9821248	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9823746	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9833387	0.81[EUR][1000 genomes];0.82[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	nsv532629	chr3:85763873-86608579	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv877115	chr3:86278951-86554319	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv834753	chr3:86386749-86546500	Enhancers Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:86428800-86430400	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr3:86428800-86430400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr3:86430000-86430600	Enhancers	iPS-20b Cell Line	embryonic stem cell
4	chr3:86430000-86431200	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr3:86430000-86431200	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr3:86430000-86431400	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr3:86430000-86431800	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr3:86430200-86431800	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr3:86430200-86431800	Enhancers	H1 Cell Line	embryonic stem cell

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