Variant report

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10228359	1.00[AFR][1000 genomes]
rs10228963	0.82[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs10231465	1.00[AFR][1000 genomes]
rs10239807	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10245825	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10272085	1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs12667769	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12668151	1.00[JPT][hapmap]
rs12669955	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12672221	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes]
rs1496765	1.00[JPT][hapmap]
rs1496766	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1496768	0.91[YRI][hapmap];1.00[AMR][1000 genomes]
rs16886265	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs16886281	0.91[YRI][hapmap];1.00[AMR][1000 genomes]
rs322000	0.82[YRI][hapmap]
rs57299049	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs57868514	1.00[AMR][1000 genomes]
rs58176565	1.00[AMR][1000 genomes]
rs73365824	1.00[AMR][1000 genomes]
rs73365854	1.00[AMR][1000 genomes]
rs73365872	1.00[AMR][1000 genomes]
rs73380280	1.00[AMR][1000 genomes]
rs73380297	1.00[AMR][1000 genomes]
rs73380299	1.00[AMR][1000 genomes]
rs73382118	1.00[AMR][1000 genomes]
rs73382133	1.00[AMR][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	nsv1022199	chr7:78054639-78469370	Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv538986	chr7:78054639-78469370	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv1019355	chr7:78319575-78399845	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv607657	chr7:78329795-78483211	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:78313800-78334200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr7:78327800-78341200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr7:78328200-78336600	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr7:78329600-78331000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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