Variant report

Variant	rs73098368
Chromosome Location	chr5:57940454-57940455
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs55719200	1.00[AMR][1000 genomes]
rs57083630	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57123442	1.00[AMR][1000 genomes]
rs58414332	1.00[AMR][1000 genomes]
rs61258317	1.00[AMR][1000 genomes]
rs6450489	1.00[AMR][1000 genomes]
rs6876683	1.00[AMR][1000 genomes]
rs73098311	1.00[AMR][1000 genomes]
rs73100304	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73100318	1.00[AMR][1000 genomes]
rs73100400	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73102351	1.00[AMR][1000 genomes]
rs73102385	1.00[AMR][1000 genomes]
rs73757811	1.00[AMR][1000 genomes]
rs73757934	1.00[AMR][1000 genomes]
rs7720795	1.00[AMR][1000 genomes]
rs7729997	1.00[AMR][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	esv2830363	chr5:57893949-58555491	Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv1029145	chr5:57905821-58141221	Active TSS Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv830311	chr5:57912546-58105636	Enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1020937	chr5:57938969-57959918	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	1 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	chr5:57933600-57944000	Weak transcription	Pancreatic Islets	Pancreatic Islet

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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