Variant report

Variant	rs34779979
Chromosome Location	chr6:73610291-73610292
allele	-/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs11962902	0.83[ASN][1000 genomes]
rs11969224	0.83[ASN][1000 genomes]
rs16883037	0.83[ASN][1000 genomes]
rs16883059	0.83[ASN][1000 genomes]
rs55892007	0.83[ASN][1000 genomes]
rs57297293	0.83[ASN][1000 genomes]
rs57695167	0.83[ASN][1000 genomes]
rs73753206	0.83[ASN][1000 genomes]
rs73753213	0.83[ASN][1000 genomes]
rs7741305	0.83[ASN][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	nsv830691	chr6:73530978-73743648	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	3 gene(s)	inside rSNPs	diseases
2	nsv886155	chr6:73551937-73649330	Enhancers Weak transcription Flanking Active TSS Strong 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	chr6:73602200-73616000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr6:73607600-73715400	Weak transcription	Primary B cells from cord blood	blood
3	chr6:73609800-73610600	Strong transcription	Primary hematopoietic stem cells short term culture	blood

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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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