Variant report

Variant	rs7664424
Chromosome Location	chr4:118342375-118342376
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10029940	0.80[ASN][1000 genomes]
rs11098393	0.81[JPT][hapmap]
rs12648816	0.96[ASN][1000 genomes]
rs12649487	0.83[ASN][1000 genomes]
rs12650869	0.92[ASN][1000 genomes]
rs13123675	0.83[ASN][1000 genomes]
rs17861852	0.82[ASN][1000 genomes]
rs17861856	0.82[ASN][1000 genomes]
rs17861857	0.82[ASN][1000 genomes]
rs17861858	0.82[ASN][1000 genomes]
rs17861881	0.91[ASN][1000 genomes]
rs17861883	0.96[ASN][1000 genomes]
rs17861890	0.93[ASN][1000 genomes]
rs17861891	0.92[ASN][1000 genomes]
rs17861906	0.92[ASN][1000 genomes]
rs17861907	0.92[ASN][1000 genomes]
rs17861908	0.92[ASN][1000 genomes]
rs17865437	0.96[ASN][1000 genomes]
rs17866964	0.96[ASN][1000 genomes]
rs17869806	0.92[ASN][1000 genomes]
rs17874735	0.93[ASN][1000 genomes]
rs4240306	0.81[ASN][1000 genomes]
rs4318720	0.84[CHB][hapmap]
rs4397069	0.83[ASN][1000 genomes]
rs4493615	0.92[ASN][1000 genomes]
rs4529127	0.83[ASN][1000 genomes]
rs4546314	0.96[ASN][1000 genomes]
rs4619965	0.96[ASN][1000 genomes]
rs6534034	0.83[ASN][1000 genomes]
rs6834348	0.81[ASN][1000 genomes]
rs6840658	0.92[ASN][1000 genomes]
rs6840964	0.92[ASN][1000 genomes]
rs6856237	0.96[ASN][1000 genomes]
rs7664551	0.84[ASN][1000 genomes]
rs7691925	0.87[JPT][hapmap];0.81[ASN][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	nsv1004858	chr4:118248984-118382051	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv427692	chr4:118262899-118437573	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv879826	chr4:118292314-118351381	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	5 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	chr4:118339800-118350800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

Quick Search:

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

what's new

Quick links