Variant report

Variant	rs6969674
Chromosome Location	chr7:18963338-18963339
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10226243	1.00[CHB][hapmap];1.00[CHD][hapmap];0.94[GIH][hapmap];0.80[JPT][hapmap];0.89[MKK][hapmap];0.90[TSI][hapmap];1.00[YRI][hapmap];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10229723	1.00[CHB][hapmap];0.84[JPT][hapmap];1.00[YRI][hapmap];0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10245874	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10246722	0.82[CHB][hapmap];0.94[GIH][hapmap];0.90[MEX][hapmap];0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10264621	0.95[CHB][hapmap];1.00[YRI][hapmap];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10280805	0.94[CEU][hapmap];0.89[CHB][hapmap];0.97[CHD][hapmap];0.94[GIH][hapmap];0.85[JPT][hapmap];1.00[MEX][hapmap];0.93[TSI][hapmap];1.00[YRI][hapmap];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13231656	1.00[GIH][hapmap];0.84[MEX][hapmap];0.80[ASN][1000 genomes]
rs13232564	1.00[YRI][hapmap];0.84[ASN][1000 genomes]
rs17140258	1.00[CHB][hapmap];1.00[YRI][hapmap];0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2066956	0.95[CHB][hapmap];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2190275	0.81[ASN][1000 genomes]
rs4721728	0.95[CHB][hapmap];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4721729	0.95[CHB][hapmap];1.00[YRI][hapmap];0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6950598	1.00[CHB][hapmap];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6950979	0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6969316	0.90[CHB][hapmap];0.87[ASN][1000 genomes]
rs6972136	1.00[GIH][hapmap];0.81[ASN][1000 genomes]
rs71524260	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7455192	0.81[ASN][1000 genomes]
rs7795954	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv498112	chr7:18677922-18991946	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv887813	chr7:18720135-18995552	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	esv2756248	chr7:18911960-18977760	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island lncRNA	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:18942000-18977400	Weak transcription	Aorta	Aorta

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