Variant report

Variant	rs73654127
Chromosome Location	chr9:102388792-102388793
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs16918660	0.92[AFR][1000 genomes]
rs16918670	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16918684	1.00[AMR][1000 genomes]
rs55736598	0.87[AFR][1000 genomes]
rs60185871	1.00[AMR][1000 genomes]
rs60506060	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73654117	0.92[AFR][1000 genomes]
rs73654123	0.92[AFR][1000 genomes]
rs73654125	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73654131	1.00[AMR][1000 genomes]
rs73654133	1.00[AMR][1000 genomes]
rs73654138	1.00[AMR][1000 genomes]
rs73654139	1.00[AMR][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	nsv529618	chr9:102227922-103044018	Flanking Bivalent TSS/Enh Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
2	nsv531599	chr9:102227922-103156864	Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
3	nsv893621	chr9:102342950-102585545	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:102387400-102389400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr9:102388600-102388800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr9:102388600-102389000	Enhancers	Primary hematopoietic stem cells short term culture	blood

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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