Variant report

Variant	rs2237781
Chromosome Location	chr7:126675050-126675051
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 73 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:69)

rs_ID	r²[population]
rs10268335	1.00[CEU][hapmap];0.91[CHB][hapmap];0.88[JPT][hapmap];0.97[EUR][1000 genomes]
rs10271115	1.00[CEU][hapmap]
rs10487464	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];0.97[EUR][1000 genomes]
rs10487465	1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[JPT][hapmap];0.97[EUR][1000 genomes]
rs10487466	1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[JPT][hapmap];0.97[EUR][1000 genomes]
rs11563503	1.00[CEU][hapmap];0.91[CHB][hapmap];0.88[JPT][hapmap];1.00[YRI][hapmap]
rs11563505	1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[JPT][hapmap];1.00[YRI][hapmap]
rs11563749	1.00[CEU][hapmap];0.91[CHB][hapmap];0.89[JPT][hapmap]
rs11563750	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];0.97[EUR][1000 genomes]
rs11563755	1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[JPT][hapmap];0.97[EUR][1000 genomes]
rs11563756	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[EUR][1000 genomes]
rs11563757	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];0.97[EUR][1000 genomes]
rs11563758	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11563759	1.00[CEU][hapmap];0.97[EUR][1000 genomes]
rs11563760	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];0.94[EUR][1000 genomes]
rs11563761	1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[JPT][hapmap];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11563762	1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[JPT][hapmap]
rs11563764	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap]
rs11563765	1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[JPT][hapmap]
rs11563766	1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[JPT][hapmap]
rs11563767	1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[JPT][hapmap]
rs11563768	1.00[CEU][hapmap]
rs11563769	1.00[CEU][hapmap]
rs11563771	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap]
rs11563772	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap]
rs11563773	1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[JPT][hapmap]
rs11563774	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11563782	0.83[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs11563787	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11563788	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs12667596	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap]
rs12669516	0.97[EUR][1000 genomes]
rs12670200	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap]
rs12670241	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap]
rs12670940	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs1419440	1.00[CEU][hapmap]
rs1419441	1.00[CEU][hapmap]
rs17644601	0.89[AMR][1000 genomes]
rs17862270	0.87[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs17862273	1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[JPT][hapmap]
rs17862275	1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[JPT][hapmap]
rs17862277	1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[JPT][hapmap];0.97[EUR][1000 genomes]
rs17863187	1.00[CEU][hapmap];1.00[YRI][hapmap];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs17863198	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap]
rs17863199	1.00[CEU][hapmap]
rs17864094	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17864106	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs17866413	1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[JPT][hapmap]
rs17867742	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs17867745	1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[JPT][hapmap]
rs17868694	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap]
rs17874838	0.97[EUR][1000 genomes]
rs2283089	0.91[CHB][hapmap]
rs2299526	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2402849	1.00[CEU][hapmap]
rs3779538	1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[JPT][hapmap]
rs3779539	1.00[CEU][hapmap]
rs3808129	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs3808130	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs3808131	0.83[CHB][hapmap];1.00[JPT][hapmap]
rs62468871	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs62468872	0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6467106	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap]
rs6467107	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap]
rs6467108	1.00[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap]
rs6467109	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap]
rs6958658	1.00[CEU][hapmap];0.91[CHB][hapmap];0.88[JPT][hapmap];0.97[EUR][1000 genomes]
rs6962580	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap]
rs7795745	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][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	esv2758132	chr7:126494789-126677843	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	esv2759562	chr7:126494789-126677843	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv427805	chr7:126494789-126677843	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv831121	chr7:126593363-126774413	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:126674000-126676000	Enhancers	Fetal Kidney	kidney
2	chr7:126674200-126675800	Enhancers	Fetal Intestine Large	intestine
3	chr7:126674400-126675400	Weak transcription	Pancreas	Pancrea
4	chr7:126674400-126675800	Enhancers	Fetal Intestine Small	intestine
5	chr7:126674600-126675600	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr7:126674600-126676000	Enhancers	Rectal Mucosa Donor 29	rectum
7	chr7:126674800-126675200	Enhancers	Liver	Liver

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