Variant report

Variant	rs4739037
Chromosome Location	chr8:63903324-63903325
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 71 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:68)

rs_ID	r²[population]
rs1031552	0.83[MEX][hapmap];0.81[AMR][1000 genomes]
rs10464903	1.00[CEU][hapmap];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10464904	1.00[CEU][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10464905	1.00[CEU][hapmap];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10957265	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs10957266	1.00[CEU][hapmap];0.83[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10957268	1.00[CEU][hapmap];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10957269	1.00[CEU][hapmap];0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs10957270	1.00[CEU][hapmap];0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12056582	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12541047	0.94[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs12541370	0.81[AMR][1000 genomes]
rs12541993	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12543020	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12543961	0.92[AMR][1000 genomes]
rs12545230	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12545245	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12546361	1.00[CEU][hapmap];0.94[MEX][hapmap]
rs12547772	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12547848	0.89[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs12548172	1.00[CEU][hapmap]
rs12548729	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12549172	0.96[AMR][1000 genomes];0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12675369	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12676348	1.00[CEU][hapmap];0.83[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12677953	0.94[MEX][hapmap];0.81[AMR][1000 genomes]
rs12677972	0.81[AMR][1000 genomes]
rs12678042	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12678214	1.00[CEU][hapmap];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12680223	0.81[AMR][1000 genomes]
rs12682112	0.81[AMR][1000 genomes]
rs12682385	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs16918945	0.80[CHD][hapmap]
rs16918948	0.80[CHD][hapmap]
rs16929963	0.94[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs16929988	0.91[AMR][1000 genomes];0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1963949	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2305558	0.81[AMR][1000 genomes]
rs3758147	1.00[CEU][hapmap];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs3780128	0.81[AMR][1000 genomes]
rs3824333	0.81[AMR][1000 genomes]
rs4310197	0.81[AMR][1000 genomes]
rs4317561	0.81[AMR][1000 genomes]
rs4404907	0.81[AMR][1000 genomes]
rs4521747	0.81[AMR][1000 genomes]
rs4534128	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4737616	1.00[CEU][hapmap]
rs4737621	0.92[AMR][1000 genomes]
rs4737625	0.81[AMR][1000 genomes]
rs4737626	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4737627	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4739028	0.90[AMR][1000 genomes]
rs4739031	0.92[AMR][1000 genomes]
rs4739032	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4739046	1.00[CEU][hapmap];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4739047	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs72658339	0.81[AMR][1000 genomes]
rs72658340	0.81[AMR][1000 genomes]
rs72658349	0.81[AMR][1000 genomes]
rs72658350	0.81[AMR][1000 genomes]
rs72658353	0.81[AMR][1000 genomes]
rs72658359	0.81[AMR][1000 genomes]
rs72658362	0.81[AMR][1000 genomes]
rs72658367	0.81[AMR][1000 genomes]
rs72658371	0.81[AMR][1000 genomes]
rs72658375	0.81[AMR][1000 genomes]
rs7818582	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs930840	1.00[CEU][hapmap];0.94[AMR][1000 genomes];0.96[EUR][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	nsv1018879	chr8:63281724-63937632	Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv1033527	chr8:63673915-64073735	Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	nsv6227	chr8:63892087-63936952	Weak transcription Strong transcription Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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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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