Variant report

Variant	rs67178951
Chromosome Location	chr3:116052643-116052644
allele	A/C/T
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:19)

rs_ID	r²[population]
rs13069010	0.84[ASN][1000 genomes]
rs13069169	0.93[ASN][1000 genomes]
rs13075678	0.84[ASN][1000 genomes]
rs13075875	0.84[ASN][1000 genomes]
rs13077535	0.84[ASN][1000 genomes]
rs13079395	1.00[ASN][1000 genomes]
rs13098368	1.00[ASN][1000 genomes]
rs13100341	0.84[ASN][1000 genomes]
rs1583182	0.84[ASN][1000 genomes]
rs17646621	0.93[ASN][1000 genomes]
rs17647031	1.00[ASN][1000 genomes]
rs17703257	1.00[ASN][1000 genomes]
rs34126529	0.93[ASN][1000 genomes]
rs34584395	1.00[ASN][1000 genomes]
rs34663845	0.95[ASN][1000 genomes]
rs35841859	0.98[ASN][1000 genomes]
rs4831094	0.89[ASN][1000 genomes]
rs4831132	0.84[ASN][1000 genomes]
rs4831139	0.84[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv877361	chr3:116017931-116138039	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr3:116046200-116058000	Weak transcription	Colon Smooth Muscle	Colon
2	chr3:116052200-116060600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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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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