Variant report

Variant	rs11120747
Chromosome Location	chr1:216438500-216438501
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10779666	0.80[CHB][hapmap];0.80[YRI][hapmap]
rs10779667	0.88[TSI][hapmap]
rs10864235	1.00[ASW][hapmap];0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.94[GIH][hapmap];0.95[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap]
rs10864237	0.86[TSI][hapmap]
rs11120752	0.80[CHB][hapmap]
rs1146766	0.95[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap]
rs12129284	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[JPT][hapmap]
rs12134474	0.80[CHB][hapmap];0.82[AMR][1000 genomes]
rs1578245	0.80[CHB][hapmap];0.90[JPT][hapmap];0.95[MEX][hapmap];0.90[TSI][hapmap];0.82[AMR][1000 genomes]
rs301761	0.95[CHB][hapmap];0.89[JPT][hapmap]
rs3754064	0.86[CEU][hapmap];0.91[MEX][hapmap];0.83[TSI][hapmap];0.81[EUR][1000 genomes]
rs3767692	0.90[CEU][hapmap]
rs385463	0.95[CHB][hapmap];0.89[JPT][hapmap]
rs386654	0.95[CHB][hapmap];0.96[CHD][hapmap];0.89[JPT][hapmap]
rs404925	0.95[CHB][hapmap];0.89[JPT][hapmap];0.91[ASN][1000 genomes]
rs4846269	0.86[TSI][hapmap]
rs680410	0.90[JPT][hapmap]
rs696719	0.86[CEU][hapmap];0.85[EUR][1000 genomes]
rs696720	0.95[CEU][hapmap];1.00[CHB][hapmap];0.90[CHD][hapmap];0.97[GIH][hapmap];0.95[JPT][hapmap];1.00[TSI][hapmap]
rs700015	0.86[CEU][hapmap];0.90[MEX][hapmap];0.83[TSI][hapmap];0.81[EUR][1000 genomes]
rs700021	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];0.95[JPT][hapmap];0.95[MEX][hapmap];1.00[TSI][hapmap]
rs700022	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.94[GIH][hapmap];0.95[JPT][hapmap];0.91[MEX][hapmap];1.00[TSI][hapmap]
rs773042	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];0.84[JPT][hapmap];0.97[TSI][hapmap]
rs810115	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap]

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	nsv1006504	chr1:215890460-216642124	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv535288	chr1:215890460-216642124	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv549199	chr1:216384908-216814702	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	4 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
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