Variant report

Variant	rs8026895
Chromosome Location	chr15:49885110-49885111
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10163097	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs56763435	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57378870	0.99[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs58370889	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58619514	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59152286	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60707261	0.83[AMR][1000 genomes]
rs61014555	0.83[AMR][1000 genomes]
rs61344016	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73404129	0.83[AMR][1000 genomes]
rs73404137	0.83[AMR][1000 genomes]
rs73404155	0.83[AMR][1000 genomes]
rs73404164	0.83[AMR][1000 genomes]
rs73404174	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73404185	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73404187	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73404198	0.83[AMR][1000 genomes]
rs73406008	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73406013	0.99[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs73406014	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74012433	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8028721	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs8030707	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9745254	0.91[AFR][1000 genomes]
rs9972316	0.99[AFR][1000 genomes];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	nsv569392	chr15:49789413-49926300	ZNF genes & repeats Flanking Active TSS Strong transcription Weak transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
2	nsv431388	chr15:49835663-49997483	Flanking Active TSS Strong transcription ZNF genes & repeats Weak transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
3	nsv1040578	chr15:49841444-49890789	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:49856200-49897400	Weak transcription	Skeletal Muscle Female	skeletal muscle
2	chr15:49866800-49897600	Weak transcription	Ovary	ovary
3	chr15:49868800-49892400	Weak transcription	Left Ventricle	heart
4	chr15:49879600-49887600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr15:49885000-49885400	ZNF genes & repeats	Spleen	Spleen
6	chr15:49885000-49885600	Active TSS	HepG2	liver

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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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