Variant report

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

rs_ID	r²[population]
rs10085736	0.88[CHB][hapmap]
rs1024559	0.88[CHB][hapmap]
rs10262559	0.81[CHB][hapmap];0.87[JPT][hapmap];0.81[ASN][1000 genomes]
rs10282605	0.81[CHB][hapmap];0.87[JPT][hapmap]
rs11971743	0.81[ASN][1000 genomes]
rs11979750	0.82[ASN][1000 genomes]
rs11979752	0.82[ASN][1000 genomes]
rs12705123	0.83[ASN][1000 genomes]
rs13232021	0.85[CEU][hapmap];0.87[CHB][hapmap];0.82[ASN][1000 genomes]
rs13235135	0.85[CEU][hapmap];0.87[CHB][hapmap];0.82[ASN][1000 genomes]
rs13239318	0.88[CHB][hapmap];0.82[ASN][1000 genomes]
rs17152161	0.85[CEU][hapmap];0.87[CHB][hapmap];0.82[ASN][1000 genomes]
rs2079469	0.80[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2237622	0.94[JPT][hapmap]
rs2528861	0.81[JPT][hapmap]
rs2528873	0.87[CHB][hapmap];0.82[ASN][1000 genomes]
rs2528875	0.94[CHB][hapmap];0.82[ASN][1000 genomes]
rs2711862	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2711865	0.81[CHB][hapmap];0.87[JPT][hapmap]
rs2711882	0.82[ASN][1000 genomes]
rs2711883	0.81[CHB][hapmap];0.82[ASN][1000 genomes]
rs2711887	0.82[ASN][1000 genomes]
rs34079239	0.93[AFR][1000 genomes];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs35603368	0.87[AFR][1000 genomes];0.80[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs3823990	0.92[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs56345626	0.83[ASN][1000 genomes]
rs7804453	0.88[CHB][hapmap];0.82[ASN][1000 genomes]
rs7808106	0.87[CHB][hapmap]

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	nsv1030446	chr7:102932689-103221638	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	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
3	nsv831085	chr7:103140672-103342388	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv888923	chr7:103143117-103199719	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:103130800-103155000	Weak transcription	Brain Substantia Nigra	brain
2	chr7:103130800-103163600	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr7:103137400-103164400	Weak transcription	Brain Anterior Caudate	brain
4	chr7:103143600-103153200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr7:103144200-103153000	Weak transcription	HepG2	liver

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