Variant report

Variant	rs72953103
Chromosome Location	chr3:70551313-70551314
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]
rs72948808	1.00[AMR][1000 genomes]
rs72948811	1.00[AMR][1000 genomes]
rs72948812	1.00[AMR][1000 genomes]
rs72951046	1.00[AMR][1000 genomes]
rs72951058	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72951060	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72951062	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7635817	0.87[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	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	chr3:70549800-70551800	Enhancers	Fetal Thymus	thymus
2	chr3:70550000-70551400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr3:70550600-70551600	Enhancers	Primary B cells from cord blood	blood
4	chr3:70550800-70551400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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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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