Variant report

Variant	rs2496437
Chromosome Location	chr13:39288321-39288322
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs11147723	0.86[JPT][hapmap]
rs11147725	0.86[JPT][hapmap]
rs2197887	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2442359	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2442366	0.84[YRI][hapmap]
rs2442373	0.82[JPT][hapmap]
rs2496433	0.81[AFR][1000 genomes]
rs2496434	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2496446	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2496448	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2496449	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2496451	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9532273	0.82[ASN][1000 genomes]
rs9548443	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9548444	0.90[ASN][1000 genomes]
rs9634754	0.83[JPT][hapmap]
rs990909	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[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	nsv832585	chr13:39233307-39424375	Weak transcription Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:39279200-39294600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
2	chr13:39282200-39293200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr13:39283400-39300200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr13:39287800-39292600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr13:39288000-39288400	Enhancers	H9 Cell Line	embryonic stem cell

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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

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