Variant report

Variant	rs13233322
Chromosome Location	chr7:18915701-18915702
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10237149	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10237280	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10237366	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10486314	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11761877	0.91[CHB][hapmap];0.95[JPT][hapmap];0.94[ASN][1000 genomes]
rs12530943	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12536081	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12699994	0.95[CHB][hapmap];0.85[JPT][hapmap];0.85[ASN][1000 genomes]
rs12699998	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12699999	0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12700000	0.89[ASN][1000 genomes]
rs12700001	0.86[EUR][1000 genomes]
rs12700002	0.80[EUR][1000 genomes]
rs12700003	0.83[CEU][hapmap];0.83[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs13242358	0.93[ASN][1000 genomes]
rs13242758	0.88[AMR][1000 genomes]
rs2028015	1.00[CHB][hapmap];0.94[JPT][hapmap];0.97[ASN][1000 genomes]
rs2286213	0.82[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs34854568	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs3852257	0.80[CHB][hapmap]
rs55761404	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs59987684	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6461387	0.82[CEU][hapmap];0.95[CHB][hapmap];0.85[JPT][hapmap];0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6461389	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6461390	0.86[CEU][hapmap];0.87[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6461391	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6461392	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6461393	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6461394	0.82[AMR][1000 genomes]
rs67248060	0.89[ASN][1000 genomes]
rs6951144	0.81[AMR][1000 genomes]
rs6951745	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6973029	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs756854	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7794241	0.82[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap];0.97[YRI][hapmap];0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7801037	0.83[AMR][1000 genomes];0.85[ASN][1000 genomes]

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	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	nsv523497	chr7:18896011-18959381	Weak transcription Flanking Active TSS Genic enhancers Enhancers ZNF genes & repeats Active TSS	TF binding region CpG island lncRNA	1 gene(s)	inside rSNPs	diseases
4	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:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:18903000-18940000	Weak transcription	Aorta	Aorta
2	chr7:18906200-18929200	Weak transcription	Left Ventricle	heart

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