Variant report

Variant	rs2269718
Chromosome Location	chr1:159275706-159275707
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs10489855	0.82[JPT][hapmap];1.00[AFR][1000 genomes]
rs12087219	0.81[JPT][hapmap]
rs12562171	1.00[AFR][1000 genomes]
rs16841957	1.00[AFR][1000 genomes]
rs16842010	1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs2269719	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56697178	0.83[EUR][1000 genomes]
rs58037016	1.00[AFR][1000 genomes]
rs58135923	0.87[EUR][1000 genomes]
rs59488253	0.93[EUR][1000 genomes]
rs61601273	1.00[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs72633670	1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv872487	chr1:159196765-159342439	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv872488	chr1:159218266-159336948	Flanking Active TSS Enhancers Weak 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	chr1:159272600-159277000	Weak transcription	Primary hematopoietic stem cells	blood
2	chr1:159273600-159277000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr1:159274200-159275800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr1:159274200-159277200	Weak transcription	Primary monocytes fromperipheralblood	blood

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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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