Variant report

Variant	rs481531
Chromosome Location	chr6:85877704-85877705
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1321748	0.83[EUR][1000 genomes]
rs1535314	0.91[EUR][1000 genomes]
rs1958939	0.91[EUR][1000 genomes]
rs1981016	0.91[EUR][1000 genomes]
rs4053810	0.83[EUR][1000 genomes]
rs4053811	0.83[EUR][1000 genomes]
rs486470	0.80[EUR][1000 genomes]
rs519667	0.89[EUR][1000 genomes]
rs535422	0.91[EUR][1000 genomes]
rs562034	0.80[EUR][1000 genomes]
rs571787	0.84[EUR][1000 genomes]
rs581803	0.84[EUR][1000 genomes]
rs593602	0.84[EUR][1000 genomes]
rs594124	0.84[EUR][1000 genomes]
rs608022	0.84[EUR][1000 genomes]
rs637870	0.91[EUR][1000 genomes]
rs7746109	0.91[EUR][1000 genomes]
rs9351055	0.91[EUR][1000 genomes]

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	nsv1017418	chr6:85344786-86259540	Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Enhancers Bivalent/Poised TSS Strong transcription Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
2	nsv538347	chr6:85344786-86259540	Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:85877600-85879000	Enhancers	iPS-18 Cell Line	embryonic stem cell

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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