Variant report

Variant	rs2791290
Chromosome Location	chr1:216542152-216542153
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10779261	0.84[CHB][hapmap];0.84[JPT][hapmap]
rs11117565	0.92[JPT][hapmap]
rs11117568	0.92[JPT][hapmap]
rs11117569	0.92[JPT][hapmap]
rs11117573	0.84[JPT][hapmap]
rs11117575	0.92[JPT][hapmap]
rs11117576	0.92[JPT][hapmap]
rs11120756	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11120757	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11801737	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11803923	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12407759	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1606357	0.88[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap]
rs17042212	0.80[CEU][hapmap];1.00[YRI][hapmap];0.80[AMR][1000 genomes]
rs1805050	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2089947	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2137402	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2669050	0.92[JPT][hapmap]
rs2669051	0.92[JPT][hapmap]
rs2669052	0.84[CHB][hapmap];0.92[JPT][hapmap]
rs2669056	0.92[JPT][hapmap]
rs2791289	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2791292	0.92[JPT][hapmap]
rs2809295	0.84[CHB][hapmap];0.92[JPT][hapmap]
rs2809297	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2809300	0.92[JPT][hapmap]
rs4085412	1.00[YRI][hapmap]
rs4253963	0.84[CHB][hapmap];0.92[JPT][hapmap]
rs4314947	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs4350256	0.91[JPT][hapmap]
rs4420153	0.84[CHB][hapmap];0.92[JPT][hapmap]
rs4431908	0.92[JPT][hapmap]
rs4443953	0.92[JPT][hapmap]
rs4488081	0.84[CHB][hapmap];0.92[JPT][hapmap]
rs4846428	0.92[JPT][hapmap]
rs4846660	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs61584034	0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7544306	0.92[JPT][hapmap]
rs7550759	0.84[CHB][hapmap];0.92[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:6 , 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
4	nsv1003815	chr1:216504235-216836498	Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
5	nsv535289	chr1:216504235-216836498	Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
6	nsv523863	chr1:216517635-216629416	Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 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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