Variant report

Variant	rs7729238
Chromosome Location	chr5:111863308-111863309
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs60579228	1.00[AMR][1000 genomes]
rs6859247	1.00[AMR][1000 genomes]
rs6867235	1.00[AMR][1000 genomes]
rs6873922	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7706970	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv599368	chr5:111399885-112032675	Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	nsv882715	chr5:111836278-111894491	Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	n/a
3	nsv882716	chr5:111848890-111894491	Active TSS Enhancers Flanking Active TSS Genic enhancers Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:111860600-111863400	Weak transcription	Adipose Nuclei	Adipose
2	chr5:111861000-111863400	Enhancers	Primary B cells from peripheral blood	blood
3	chr5:111861200-111868200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
4	chr5:111861600-111868000	Weak transcription	GM12878-XiMat	blood
5	chr5:111861600-111868200	Weak transcription	Primary B cells from cord blood	blood
6	chr5:111862400-111868400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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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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