Variant report

Variant	rs72948808
Chromosome Location	chr3:70575880-70575881
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs72948811	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72948812	1.00[AMR][1000 genomes]
rs72951046	1.00[AMR][1000 genomes]
rs72951058	1.00[AMR][1000 genomes]
rs72951060	1.00[AMR][1000 genomes]
rs72951062	1.00[AMR][1000 genomes]
rs72953103	1.00[AMR][1000 genomes]
rs7635817	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	nsv999046	chr3:70549472-70576944	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:70570200-70576000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
2	chr3:70570200-70580800	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr3:70575800-70576600	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr3:70575800-70576600	Enhancers	iPS-15b Cell Line	embryonic stem cell

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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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