Variant report

Variant	rs13267723
Chromosome Location	chr8:130672344-130672345
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs34271371	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs34547718	0.91[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs4448234	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs55719299	0.91[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs7006796	0.80[EUR][1000 genomes]
rs71522551	0.82[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	nsv891446	chr8:130656205-130710638	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:130671600-130673200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr8:130671600-130673200	Weak transcription	Dnd41	blood
3	chr8:130671600-130673400	Weak transcription	K562	blood
4	chr8:130672000-130674000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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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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