Variant report

Variant	rs73434992
Chromosome Location	chr11:24690191-24690192
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10742047	1.00[EUR][1000 genomes]
rs11028116	1.00[EUR][1000 genomes]
rs11028140	1.00[EUR][1000 genomes]
rs12270550	1.00[EUR][1000 genomes]
rs12279481	1.00[EUR][1000 genomes]
rs12280090	1.00[EUR][1000 genomes]
rs12281099	1.00[EUR][1000 genomes]
rs12295428	1.00[EUR][1000 genomes]
rs1396845	1.00[EUR][1000 genomes]
rs1396847	1.00[EUR][1000 genomes]
rs1858159	1.00[EUR][1000 genomes]
rs57637255	1.00[EUR][1000 genomes]
rs6484055	1.00[EUR][1000 genomes]
rs6484056	1.00[EUR][1000 genomes]
rs73434995	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73434997	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9919580	1.00[EUR][1000 genomes]
rs9919604	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1055026	chr11:24151133-24737122	Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1037744	chr11:24174588-24737122	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv897093	chr11:24675207-24736493	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr11:24686200-24691200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr11:24687400-24690400	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr11:24689800-24690400	Enhancers	iPS-20b Cell Line	embryonic stem cell
4	chr11:24689800-24692000	Enhancers	HUES48 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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