Variant report

Variant	rs10253325
Chromosome Location	chr7:14486957-14486958
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10271285	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10499440	0.85[CEU][hapmap]
rs10950525	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs10950526	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs11525791	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap]
rs11526188	0.85[CEU][hapmap]
rs11977908	0.85[CEU][hapmap]
rs11978895	1.00[CEU][hapmap]
rs12531006	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs12532388	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs12533433	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs12533729	0.86[EUR][1000 genomes]
rs12534446	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap]
rs12538874	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs12540646	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs12540892	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs1367775	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs1431533	0.86[EUR][1000 genomes]
rs17168175	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs17168177	0.86[EUR][1000 genomes]
rs17168203	0.85[CEU][hapmap]
rs171926	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17651138	0.85[CEU][hapmap]
rs17651211	0.85[CEU][hapmap]
rs1835676	0.96[EUR][1000 genomes]
rs1835677	0.96[EUR][1000 genomes]
rs183808	0.96[EUR][1000 genomes]
rs196750	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs196753	1.00[CEU][hapmap];0.90[AFR][1000 genomes];0.97[EUR][1000 genomes]
rs196760	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap]
rs2116317	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs2116318	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs2163509	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs58759714	0.95[EUR][1000 genomes]
rs59778011	0.96[EUR][1000 genomes]
rs60294470	0.95[EUR][1000 genomes]
rs62443273	0.96[EUR][1000 genomes]
rs9639198	0.85[CEU][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	nsv949033	chr7:14086106-14860323	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv915603	chr7:14443884-14624268	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	esv1848567	chr7:14464118-14579801	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv887707	chr7:14471682-14576163	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:14486200-14487600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
2	chr7:14486400-14487600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
3	chr7:14486600-14487000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
4	chr7:14486600-14487200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
5	chr7:14486600-14487400	Enhancers	Primary T cells from cord blood	blood

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