Variant report

Variant	rs73683567
Chromosome Location	chr8:69477662-69477663
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs1400551	1.00[EUR][1000 genomes]
rs16934575	1.00[EUR][1000 genomes]
rs16934578	1.00[EUR][1000 genomes]
rs58125593	1.00[EUR][1000 genomes]
rs6981953	1.00[EUR][1000 genomes]
rs6999119	1.00[EUR][1000 genomes]
rs72664912	1.00[EUR][1000 genomes]
rs72664918	1.00[EUR][1000 genomes]
rs72664937	1.00[EUR][1000 genomes]
rs72664939	1.00[EUR][1000 genomes]
rs72664940	1.00[EUR][1000 genomes]
rs72664943	1.00[EUR][1000 genomes]
rs72664944	1.00[EUR][1000 genomes]
rs73683565	1.00[EUR][1000 genomes]
rs7827049	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948687	chr8:69041121-69642540	Flanking Bivalent TSS/Enh Enhancers Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv890981	chr8:69413110-69534542	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv1023815	chr8:69442474-69486856	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv890983	chr8:69447339-69503062	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:69468400-69478600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr8:69476800-69477800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr8:69477400-69477800	Enhancers	H9 Cell Line	embryonic stem cell
4	chr8:69477400-69478000	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr8:69477400-69478000	Enhancers	H1 Cell Line	embryonic stem cell
6	chr8:69477400-69478000	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr8:69477400-69478200	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr8:69477400-69478800	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr8:69477400-69478800	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr8:69477600-69478000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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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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