Variant report

Variant	rs2952687
Chromosome Location	chr7:112258700-112258701
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10224255	0.83[ASN][1000 genomes]
rs1234346	0.94[CHB][hapmap];0.86[ASN][1000 genomes]
rs1234348	0.80[CEU][hapmap];0.94[CHB][hapmap];0.80[JPT][hapmap];0.89[ASN][1000 genomes]
rs1234350	0.82[EUR][1000 genomes]
rs1234351	0.89[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1234352	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1234383	0.91[ASN][1000 genomes]
rs1236840	0.82[ASN][1000 genomes]
rs1613412	0.90[ASN][1000 genomes]
rs1623536	0.85[ASN][1000 genomes]
rs1796502	0.82[CHB][hapmap];0.89[JPT][hapmap];0.94[ASN][1000 genomes]
rs1922899	0.81[ASN][1000 genomes]
rs1922902	0.81[ASN][1000 genomes]
rs2079530	0.84[CEU][hapmap];0.94[CHB][hapmap];0.85[ASN][1000 genomes]
rs2097672	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2188547	0.85[AFR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2188550	0.81[ASN][1000 genomes]
rs2860402	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs28844	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2905278	0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2905280	0.94[CEU][hapmap];0.94[CHB][hapmap];0.90[JPT][hapmap]
rs2905285	0.84[ASN][1000 genomes]
rs2952678	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2952688	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];1.00[YRI][hapmap]
rs2966480	0.84[ASN][1000 genomes]
rs2966483	0.81[ASN][1000 genomes]
rs3111438	0.82[ASN][1000 genomes]
rs3128399	0.82[ASN][1000 genomes]
rs4473967	0.84[ASN][1000 genomes]
rs4518580	0.80[CEU][hapmap];0.94[CHB][hapmap];0.90[JPT][hapmap];0.89[ASN][1000 genomes]
rs977478	0.81[ASN][1000 genomes]
rs977479	0.83[ASN][1000 genomes]
rs977480	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531436	chr7:111856171-112585407	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	105 gene(s)	inside rSNPs	diseases
2	nsv889055	chr7:112174089-112353440	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 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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