Variant report

Variant	rs6775945
Chromosome Location	chr3:78291672-78291673
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs13069858	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13072134	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs13075203	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs13075352	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13089281	0.93[EUR][1000 genomes]
rs13100216	1.00[EUR][1000 genomes]
rs34664724	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs34794178	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35161856	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs35639730	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs36118920	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6775712	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6788678	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs71324619	0.93[EUR][1000 genomes]
rs71324620	0.93[EUR][1000 genomes]
rs71324621	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs71324622	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs71324623	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs71324624	1.00[EUR][1000 genomes]
rs71324625	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs71324626	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs867064	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv877017	chr3:77881397-78670654	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv1008290	chr3:77895292-78308583	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv536595	chr3:77895292-78308583	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv529995	chr3:78188643-78739698	Enhancers Weak transcription Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 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	chr3:78281000-78295400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr3:78289800-78291800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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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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