Variant report

Variant	rs7148606
Chromosome Location	chr14:72408692-72408693
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs17093752	0.89[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs2190864	0.91[EUR][1000 genomes]
rs2190873	0.85[EUR][1000 genomes]
rs2191251	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2238284	0.89[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs2332687	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs36318	0.95[ASN][1000 genomes]
rs36332	0.83[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs36341	0.81[EUR][1000 genomes]
rs6574035	0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.99[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	nsv530794	chr14:72113818-73034008	Enhancers Bivalent/Poised TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:72407600-72409200	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr14:72408400-72409400	Enhancers	GM12878-XiMat	blood
3	chr14:72408600-72409400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr14:72408600-72412600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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