Variant report

Variant	rs57648524
Chromosome Location	chr8:65388792-65388793
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs16931204	1.00[AMR][1000 genomes]
rs59268308	1.00[AMR][1000 genomes]
rs60050156	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73234041	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73248329	1.00[AMR][1000 genomes]
rs73248339	1.00[AMR][1000 genomes]
rs73248367	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73248371	0.92[AFR][1000 genomes];1.00[AMR][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	nsv534001	chr8:64992196-65798776	Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 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	chr8:65386400-65389600	Enhancers	HMEC	breast
2	chr8:65387800-65393400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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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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