Variant report

Variant	rs73963936
Chromosome Location	chr2:145505795-145505796
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs55647125	0.93[AFR][1000 genomes]
rs55665103	0.93[AFR][1000 genomes]
rs55701936	0.81[AFR][1000 genomes]
rs55992490	0.93[AFR][1000 genomes]
rs56049026	0.93[AFR][1000 genomes]
rs56824932	0.93[AFR][1000 genomes]
rs57273989	0.93[AFR][1000 genomes]
rs59274820	0.81[AFR][1000 genomes]
rs59373132	0.81[AFR][1000 genomes]
rs60328211	0.85[AFR][1000 genomes]
rs61697170	0.81[AFR][1000 genomes]
rs71428044	0.89[AFR][1000 genomes]
rs73962084	0.81[AFR][1000 genomes]
rs73962088	0.81[AFR][1000 genomes]
rs73962089	0.93[AFR][1000 genomes]
rs73962094	0.93[AFR][1000 genomes]
rs73962096	0.93[AFR][1000 genomes]
rs73962101	0.93[AFR][1000 genomes]
rs73963909	0.81[AFR][1000 genomes]
rs73963910	0.81[AFR][1000 genomes]
rs73963912	0.93[AFR][1000 genomes]
rs73963913	0.93[AFR][1000 genomes]
rs73963914	0.93[AFR][1000 genomes]
rs73963915	0.93[AFR][1000 genomes]
rs73963917	0.93[AFR][1000 genomes]
rs73963918	0.93[AFR][1000 genomes]
rs73963920	0.81[AFR][1000 genomes]
rs73963921	0.93[AFR][1000 genomes]
rs73963922	0.81[AFR][1000 genomes]
rs73963923	0.93[AFR][1000 genomes]
rs73963924	0.93[AFR][1000 genomes]
rs73963925	0.93[AFR][1000 genomes]
rs73963926	0.93[AFR][1000 genomes]
rs73963931	1.00[AFR][1000 genomes]
rs73963934	0.89[AFR][1000 genomes]
rs73963938	0.89[AFR][1000 genomes]
rs73963941	0.93[AFR][1000 genomes]
rs73963943	0.81[AFR][1000 genomes]
rs73963945	0.93[AFR][1000 genomes]
rs73963947	0.93[AFR][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	nsv1002563	chr2:145182201-145863253	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
2	nsv535957	chr2:145182201-145863253	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
3	nsv834397	chr2:145439528-145608628	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 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	chr2:145505400-145506400	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
2	chr2:145505400-145506600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr2:145505600-145506800	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood

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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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