Variant report

Variant	rs7327672
Chromosome Location	chr13:61913655-61913656
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs12863764	0.81[ASN][1000 genomes]
rs1411568	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2039209	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9317184	0.81[ASN][1000 genomes]
rs9528317	0.85[ASN][1000 genomes]
rs9528321	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9539097	0.91[ASN][1000 genomes]
rs9539098	0.91[ASN][1000 genomes]
rs9539110	0.94[ASN][1000 genomes]
rs9539111	0.91[ASN][1000 genomes]
rs9539125	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9539126	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9539129	0.83[AMR][1000 genomes];0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9539130	0.83[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs9539135	0.81[ASN][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	nsv900245	chr13:61873379-62057698	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv455904	chr13:61883623-61953406	ZNF genes & repeats Weak transcription Active TSS Enhancers Genic enhancers Strong transcription	n/a	n/a	inside rSNPs	diseases
3	nsv561867	chr13:61883623-61953406	Active TSS Enhancers Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	n/a	n/a	inside rSNPs	diseases
4	nsv948661	chr13:61906251-62179649	Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:61913000-61913800	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr13:61913600-61916000	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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