Variant report

Variant	rs6866382
Chromosome Location	chr5:118060629-118060630
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs1019453	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1473337	1.00[CEU][hapmap]
rs17144589	1.00[EUR][1000 genomes]
rs59610600	1.00[EUR][1000 genomes]
rs59722126	1.00[EUR][1000 genomes]
rs61214571	1.00[EUR][1000 genomes]
rs6886099	1.00[EUR][1000 genomes]
rs73236957	1.00[EUR][1000 genomes]
rs73251303	1.00[EUR][1000 genomes]
rs73251311	1.00[EUR][1000 genomes]
rs73251313	1.00[EUR][1000 genomes]
rs73251382	1.00[EUR][1000 genomes]
rs73251385	1.00[EUR][1000 genomes]
rs73253507	1.00[EUR][1000 genomes]
rs7448288	1.00[EUR][1000 genomes]
rs7722494	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs7727078	0.94[AFR][1000 genomes]
rs7734451	1.00[EUR][1000 genomes]

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	nsv1032241	chr5:117900051-118157400	Weak transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv882767	chr5:117931730-118385691	Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Enhancers Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
3	nsv599561	chr5:118043996-118073157	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	lncRNA	n/a	inside rSNPs	n/a
4	nsv1034487	chr5:118047803-118085925	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	n/a

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:118058400-118062400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr5:118059200-118062800	Weak transcription	Fetal Lung	lung

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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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