Variant report

Variant	rs10280805
Chromosome Location	chr7:18966742-18966743
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10226243	1.00[ASW][hapmap];0.89[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];0.85[JPT][hapmap];1.00[LWK][hapmap];0.90[MKK][hapmap];0.90[TSI][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10229723	0.89[CHB][hapmap];0.90[JPT][hapmap];1.00[YRI][hapmap];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10245874	0.85[JPT][hapmap];0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10246722	0.82[CHB][hapmap];0.81[CHD][hapmap];0.88[GIH][hapmap];0.89[MEX][hapmap];0.83[TSI][hapmap];0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10264621	0.94[CHB][hapmap];0.85[JPT][hapmap];1.00[YRI][hapmap];0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13231656	0.94[GIH][hapmap];0.83[MEX][hapmap]
rs13232564	0.83[CHB][hapmap];1.00[YRI][hapmap];0.85[ASN][1000 genomes]
rs17140258	0.89[CHB][hapmap];0.85[JPT][hapmap];1.00[YRI][hapmap];0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2066956	0.84[CHB][hapmap];0.81[JPT][hapmap];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4721728	0.84[CEU][hapmap];0.84[CHB][hapmap];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4721729	0.84[CHB][hapmap];0.81[JPT][hapmap];1.00[YRI][hapmap];0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6950598	0.89[CHB][hapmap];0.81[JPT][hapmap];0.93[ASN][1000 genomes]
rs6950979	0.86[ASN][1000 genomes]
rs6969316	0.80[JPT][hapmap];0.85[ASN][1000 genomes]
rs6969674	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]
rs6972136	0.94[GIH][hapmap];0.82[ASN][1000 genomes]
rs71524260	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7455192	0.82[ASN][1000 genomes]
rs7795954	0.80[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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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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