Variant report

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10499176	1.00[CEU][hapmap]
rs10499178	1.00[CEU][hapmap]
rs17059617	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17059726	1.00[CEU][hapmap]
rs17059735	1.00[CEU][hapmap]
rs17059739	1.00[CEU][hapmap]
rs17059760	1.00[CEU][hapmap]
rs17059787	1.00[CEU][hapmap]
rs17059799	1.00[CEU][hapmap]
rs17059801	1.00[CEU][hapmap]
rs17059808	1.00[CEU][hapmap]
rs17059810	1.00[CEU][hapmap]
rs17059851	1.00[CEU][hapmap]
rs17059853	1.00[CEU][hapmap]
rs17059909	1.00[CEU][hapmap]
rs1999473	1.00[CEU][hapmap]
rs2275064	1.00[CEU][hapmap]
rs2281488	0.86[AMR][1000 genomes]
rs3777433	1.00[CEU][hapmap]
rs3777444	1.00[CEU][hapmap]
rs3777448	1.00[CEU][hapmap]
rs3777451	1.00[CEU][hapmap]
rs3777456	1.00[CEU][hapmap]
rs3822859	1.00[CEU][hapmap]
rs57211621	0.86[AMR][1000 genomes]
rs714709	1.00[CEU][hapmap]
rs7762679	0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533971	chr6:130490694-131172051	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	nsv604664	chr6:131004998-131115817	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv1025019	chr6:131074711-131116070	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv604665	chr6:131077027-131115817	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv604666	chr6:131078180-131122295	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:131110200-131113200	Weak transcription	HepG2	liver
2	chr6:131111000-131117000	Weak transcription	Lung	lung
3	chr6:131111200-131115000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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