Variant report

Variant	rs73030812
Chromosome Location	chr1:159775916-159775917
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs11265281	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12087590	0.82[AFR][1000 genomes]
rs12094789	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59177920	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59515106	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60197485	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60366237	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60865130	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6666384	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6670357	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6670761	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6681603	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6682005	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6699933	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73028940	0.86[AFR][1000 genomes]
rs73028944	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73028947	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73030807	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73030810	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73030816	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73030822	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1005195	chr1:159452759-159910337	Active TSS Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
2	nsv521503	chr1:159762120-159795478	Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 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	chr1:159771000-159776600	Weak transcription	Primary T cells from cord blood	blood
2	chr1:159772800-159777400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr1:159772800-159778800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr1:159773400-159776800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
5	chr1:159774000-159776400	Enhancers	Primary T cells fromperipheralblood	blood
6	chr1:159774600-159779000	Weak transcription	Spleen	Spleen
7	chr1:159774800-159796000	Weak transcription	Right Atrium	heart
8	chr1:159775400-159777600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr1:159775400-159779400	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
10	chr1:159775800-159793400	Weak transcription	Primary T killer memory cells from peripheral blood	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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