Variant report

Variant	rs219264
Chromosome Location	chr7:150994093-150994094
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs219245	0.81[ASN][1000 genomes]
rs219246	0.81[ASN][1000 genomes]
rs219247	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs219248	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs219249	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs219263	0.82[ASN][1000 genomes]
rs219265	0.80[ASN][1000 genomes]
rs219267	0.82[ASN][1000 genomes]
rs219268	0.82[ASN][1000 genomes]
rs219269	0.82[ASN][1000 genomes]
rs219270	0.82[ASN][1000 genomes]
rs219271	0.82[ASN][1000 genomes]
rs219272	0.82[ASN][1000 genomes]
rs219273	0.82[ASN][1000 genomes]
rs2429246	0.80[ASN][1000 genomes]
rs2429247	0.80[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	nsv1023436	chr7:150967147-150997692	Active TSS Enhancers Weak transcription Strong transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	6 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	chr7:150994000-151000400	Weak transcription	Right Atrium	heart

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dbSNP/dbVar ID: rs12345 /nsv7879
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