Variant report

Variant	rs34805714
Chromosome Location	chr8:104018101-104018102
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs11773935	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11776102	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11776378	0.80[EUR][1000 genomes]
rs11778351	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11781860	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11987421	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs13249382	0.88[EUR][1000 genomes]
rs13249414	0.85[EUR][1000 genomes]
rs13257502	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs13258117	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1512349	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs35746971	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs35956387	0.82[AMR][1000 genomes];0.87[EUR][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	esv33118	chr8:103358567-104068172	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	145 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	chr8:104018000-104022800	Weak transcription	Pancreas	Pancrea

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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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