Variant report

Variant	rs6588604
Chromosome Location	chr1:56486751-56486752
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs56248222	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56394331	1.00[AMR][1000 genomes]
rs58180102	1.00[AMR][1000 genomes]
rs59073332	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59121815	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59641326	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59741771	1.00[AMR][1000 genomes]
rs61213965	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6689869	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74072808	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74072853	1.00[AMR][1000 genomes]
rs74072892	1.00[AMR][1000 genomes]
rs74072896	1.00[AMR][1000 genomes]
rs74075204	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74075209	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74075217	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74075221	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74075222	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74075224	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74075225	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74075226	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74075233	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74075234	1.00[AFR][1000 genomes];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	nsv870513	chr1:56407227-56493106	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 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	chr1:56485200-56489400	Weak transcription	Placenta	Placenta
2	chr1:56485200-56501800	Weak transcription	Aorta	Aorta

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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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