Variant report

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10257295	1.00[JPT][hapmap]
rs10269791	1.00[JPT][hapmap]
rs11979780	1.00[JPT][hapmap]
rs17154257	1.00[JPT][hapmap]
rs2072405	1.00[CHB][hapmap]
rs2285335	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2299361	1.00[JPT][hapmap]
rs2299362	1.00[JPT][hapmap]
rs2382881	1.00[JPT][hapmap]
rs2382882	1.00[JPT][hapmap]
rs3757736	1.00[JPT][hapmap]
rs476736	1.00[JPT][hapmap]
rs491170	1.00[JPT][hapmap]
rs491921	1.00[JPT][hapmap]
rs496801	1.00[JPT][hapmap]
rs499998	1.00[JPT][hapmap]
rs549743	1.00[JPT][hapmap]
rs588423	1.00[JPT][hapmap]
rs636187	1.00[JPT][hapmap]
rs638355	1.00[JPT][hapmap]
rs651488	1.00[JPT][hapmap]
rs665251	1.00[JPT][hapmap]
rs682018	1.00[JPT][hapmap]
rs683360	1.00[JPT][hapmap]
rs6958285	1.00[JPT][hapmap]
rs7810686	1.00[JPT][hapmap]
rs7811905	1.00[JPT][hapmap]
rs9986712	1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv491911	chr7:102967150-103403622	Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv427799	chr7:103250733-103454202	Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:103390000-103434000	Weak transcription	K562	blood
2	chr7:103391000-103393400	Strong transcription	HepG2	liver
3	chr7:103391800-103392400	Enhancers	Fetal Brain Male	brain

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