Variant report

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

rs_ID	r²[population]
rs10226456	0.83[ASN][1000 genomes]
rs10235696	0.86[ASN][1000 genomes]
rs10236552	0.81[ASN][1000 genomes]
rs10238498	0.83[ASN][1000 genomes]
rs10247944	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10257360	0.83[ASN][1000 genomes]
rs10273609	0.83[ASN][1000 genomes]
rs10274240	0.83[ASN][1000 genomes]
rs10280365	0.83[ASN][1000 genomes]
rs10281485	0.81[ASN][1000 genomes]
rs12670275	0.83[ASN][1000 genomes]
rs2285533	0.81[ASN][1000 genomes]
rs28546781	0.85[ASN][1000 genomes]
rs28587189	0.83[ASN][1000 genomes]
rs34083033	0.86[ASN][1000 genomes]
rs35756879	0.84[ASN][1000 genomes]
rs35894637	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs35988800	0.83[ASN][1000 genomes]
rs57624778	0.84[EUR][1000 genomes]
rs6968540	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs73184014	0.87[EUR][1000 genomes]
rs73184016	0.88[EUR][1000 genomes]
rs73184018	0.88[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831086	chr7:104422503-104596766	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 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	chr7:104509800-104524400	Weak transcription	Pancreas	Pancrea
2	chr7:104511600-104519600	Weak transcription	Fetal Intestine Large	intestine
3	chr7:104512000-104524000	Weak transcription	Duodenum Mucosa	Duodenum
4	chr7:104516000-104519600	Weak transcription	Fetal Intestine Small	intestine

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