Variant report

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10131136	0.85[CHB][hapmap];1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs10132085	1.00[CEU][hapmap]
rs10132376	1.00[CEU][hapmap]
rs10138082	0.82[CEU][hapmap]
rs10138731	1.00[CEU][hapmap]
rs10141923	1.00[CEU][hapmap]
rs10145600	0.82[CEU][hapmap]
rs10147304	0.82[CEU][hapmap]
rs10873318	1.00[CEU][hapmap]
rs11845483	0.82[CEU][hapmap]
rs12323467	1.00[CEU][hapmap]
rs12431997	1.00[CEU][hapmap]
rs12432145	1.00[CEU][hapmap]
rs12432323	1.00[CEU][hapmap]
rs12435491	1.00[CEU][hapmap]
rs12435510	1.00[CEU][hapmap]
rs12436134	1.00[CEU][hapmap]
rs12437077	1.00[CEU][hapmap]
rs12590068	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs17107968	0.82[CEU][hapmap]
rs2370825	1.00[CEU][hapmap]
rs60875059	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7143484	0.80[ASN][1000 genomes]
rs7146567	0.85[CHB][hapmap];1.00[JPT][hapmap]
rs7160080	1.00[CEU][hapmap]
rs8005495	1.00[JPT][hapmap]
rs8017049	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs8018456	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs8018626	1.00[CEU][hapmap]
rs8021089	0.82[CEU][hapmap]

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	esv2760000	chr14:78875607-79173528	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	esv2758363	chr14:78903610-79173528	Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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