Variant report

Variant	rs73594674
Chromosome Location	chr11:102603800-102603801
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs58072368	0.95[AFR][1000 genomes]
rs73584625	0.87[AFR][1000 genomes]
rs73584665	0.87[AFR][1000 genomes]
rs73584681	0.87[AFR][1000 genomes]
rs73584695	0.87[AFR][1000 genomes]
rs73586612	0.87[AFR][1000 genomes]
rs73588692	0.83[AFR][1000 genomes]
rs73590676	0.91[AFR][1000 genomes]
rs73590699	0.91[AFR][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	nsv832252	chr11:102445479-102627879	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:102602200-102606600	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr11:102603200-102604000	Enhancers	Primary neutrophils fromperipheralblood	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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