Variant report

Variant	rs7756533
Chromosome Location	chr6:101749938-101749939
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs1485836	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1749234	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2629986	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs283184	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs283212	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs366894	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs518540	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs522795	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs613750	0.92[AMR][1000 genomes]
rs644521	0.92[AMR][1000 genomes]
rs649371	0.92[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	nsv1020400	chr6:101172705-101981665	Weak transcription Bivalent/Poised TSS Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	nsv538390	chr6:101172705-101981665	Flanking Active TSS Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:101744600-101750600	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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