Variant report

Variant	rs58359448
Chromosome Location	chr1:166324050-166324051
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs10494454	1.00[AMR][1000 genomes]
rs16856657	1.00[AMR][1000 genomes]
rs16856676	1.00[AMR][1000 genomes]
rs16856694	1.00[AMR][1000 genomes]
rs59283985	1.00[AMR][1000 genomes]
rs6677013	1.00[AMR][1000 genomes]
rs73032914	1.00[AMR][1000 genomes]
rs7529805	1.00[AMR][1000 genomes]
rs7531693	1.00[AMR][1000 genomes]
rs7531868	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	nsv916491	chr1:166000783-166948513	Bivalent/Poised TSS Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:166320600-166324400	Enhancers	Liver	Liver
2	chr1:166323600-166324400	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr1:166324000-166325200	Enhancers	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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