Variant report

Variant	rs7526462
Chromosome Location	chr1:168909952-168909953
allele	C/T
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]
rs12084554	1.00[CHD][hapmap]
rs1960548	1.00[CEU][hapmap]
rs2146195	1.00[CHD][hapmap];1.00[GIH][hapmap]
rs2419685	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2900886	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2984603	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2984604	0.93[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2984605	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2984606	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2984608	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2984609	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2984610	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2984612	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs3007398	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6427166	1.00[CEU][hapmap]
rs6427167	1.00[CEU][hapmap]
rs7514682	1.00[CEU][hapmap];1.00[JPT][hapmap];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	nsv869415	chr1:168467284-169153863	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	44 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:168908000-168910000	Enhancers	Hela-S3	cervix
2	chr1:168908600-168910200	Enhancers	Duodenum Mucosa	Duodenum
3	chr1:168908600-168910200	Enhancers	Stomach Mucosa	stomach
4	chr1:168909400-168914600	Weak transcription	Fetal Heart	heart
5	chr1:168909600-168914400	Weak transcription	Fetal Intestine Small	intestine
6	chr1:168909800-168910000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr1:168909800-168914400	Weak transcription	Fetal Intestine Large	intestine

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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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