Variant report

Variant	rs10002096
Chromosome Location	chr4:21739559-21739560
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10021133	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10029040	0.82[ASN][1000 genomes]
rs10516398	0.82[ASN][1000 genomes]
rs11725634	0.82[ASN][1000 genomes]
rs11725680	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11730531	0.82[ASN][1000 genomes]
rs11737531	0.82[ASN][1000 genomes]
rs11944162	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs13115987	0.82[ASN][1000 genomes]
rs13146273	0.82[ASN][1000 genomes]
rs13147352	0.82[ASN][1000 genomes]
rs1380271	0.82[ASN][1000 genomes]
rs1380272	0.82[ASN][1000 genomes]
rs17496681	0.82[ASN][1000 genomes]
rs17496959	0.82[ASN][1000 genomes]
rs17497844	0.82[ASN][1000 genomes]
rs17497900	0.82[ASN][1000 genomes]
rs17563311	0.82[ASN][1000 genomes]
rs17563769	0.82[ASN][1000 genomes]
rs17563824	0.82[ASN][1000 genomes]
rs1824368	0.82[ASN][1000 genomes]
rs34099045	0.82[ASN][1000 genomes]
rs34945659	0.82[ASN][1000 genomes]
rs35842590	0.82[ASN][1000 genomes]
rs60628330	0.82[ASN][1000 genomes]
rs7684151	0.82[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	nsv817467	chr4:21602921-22422816	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv878751	chr4:21712050-21793807	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:21737600-21754000	Weak transcription	Fetal Heart	heart
2	chr4:21739200-21741600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood

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