Variant report

Variant	rs72960366
Chromosome Location	chr4:147853531-147853532
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs2043703	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2304535	0.90[EUR][1000 genomes]
rs67969370	0.93[AFR][1000 genomes]
rs72943804	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72943833	1.00[AMR][1000 genomes];1.00[EUR][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	esv2456671	chr4:147852567-147853859	Enhancers Weak transcription	TF binding region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:147851600-147853600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr4:147852200-147853600	Enhancers	Primary hematopoietic stem cells	blood
3	chr4:147852200-147853600	Enhancers	Primary hematopoietic stem cells short term culture	blood
4	chr4:147853000-147853600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr4:147853200-147853800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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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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