Variant report

Variant	rs13255149
Chromosome Location	chr8:114307405-114307406
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10088226	0.90[JPT][hapmap]
rs10094251	0.93[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap]
rs10104117	0.93[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap]
rs10111510	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10505202	0.93[CHB][hapmap];1.00[JPT][hapmap]
rs10505203	0.86[CHB][hapmap];0.89[JPT][hapmap]
rs10955648	0.80[CHB][hapmap];0.91[JPT][hapmap]
rs11778054	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs11984724	0.93[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap]
rs11986420	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs11995255	0.87[CHB][hapmap];0.90[JPT][hapmap]
rs11996690	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs11997737	0.93[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap]
rs12334397	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.85[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs12674571	0.87[CHB][hapmap];0.90[JPT][hapmap]
rs12675523	0.81[CHB][hapmap];0.90[JPT][hapmap]
rs12678760	0.92[CHB][hapmap];0.90[JPT][hapmap]
rs12680523	0.89[JPT][hapmap]
rs12681814	0.82[ASN][1000 genomes]
rs12682363	0.92[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap]
rs1480445	0.81[CHB][hapmap];0.90[JPT][hapmap]
rs1480461	0.87[CHB][hapmap];1.00[JPT][hapmap]
rs1568552	0.80[CHB][hapmap];0.91[JPT][hapmap];0.82[ASN][1000 genomes]
rs16884331	0.89[JPT][hapmap]
rs16884442	0.87[CHB][hapmap];0.90[JPT][hapmap]
rs16884503	0.93[CHB][hapmap];0.90[JPT][hapmap]
rs16884505	0.92[ASN][1000 genomes]
rs16884531	0.87[CHB][hapmap];0.90[JPT][hapmap]
rs16884568	0.86[CHB][hapmap];0.90[JPT][hapmap]
rs16892635	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1879739	0.80[CHB][hapmap];0.91[JPT][hapmap];0.82[YRI][hapmap];0.82[ASN][1000 genomes]
rs1879740	0.80[CHB][hapmap];0.91[JPT][hapmap]
rs28470386	0.90[JPT][hapmap]
rs3967800	0.89[JPT][hapmap]
rs4551388	0.90[JPT][hapmap]
rs4607648	0.88[CHB][hapmap];0.90[JPT][hapmap]
rs4876512	0.93[CHB][hapmap];1.00[JPT][hapmap]
rs55810383	0.90[ASN][1000 genomes]
rs61239354	0.85[ASN][1000 genomes]
rs6981954	0.91[JPT][hapmap]
rs6993801	0.93[CHB][hapmap];1.00[JPT][hapmap]
rs6995851	0.87[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs7012235	0.93[CHB][hapmap];1.00[JPT][hapmap]
rs72670752	0.92[ASN][1000 genomes]
rs7460075	0.86[CHB][hapmap];0.90[JPT][hapmap]
rs7817251	0.89[ASN][1000 genomes]
rs7823590	0.93[CHB][hapmap];1.00[JPT][hapmap]
rs7843856	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9649936	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2754581	chr8:114029421-114419106	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv831428	chr8:114102983-114320802	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv916637	chr8:114116303-114338450	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv1022803	chr8:114180224-114354093	Enhancers Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	1 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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