Variant report

Variant	rs359892
Chromosome Location	chr2:185497327-185497328
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:185490085..185492115-chr2:185496975..185498894,2	K562	blood:

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs1014959	0.83[ASN][1000 genomes]
rs10197925	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10198049	0.82[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap]
rs10203158	0.89[CEU][hapmap];0.88[CHB][hapmap];0.80[AFR][1000 genomes];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1021043	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11890128	0.83[ASN][1000 genomes]
rs11891662	1.00[JPT][hapmap]
rs11900132	1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs12693381	0.91[CEU][hapmap];0.83[CHB][hapmap];0.80[AFR][1000 genomes];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12693383	0.92[CEU][hapmap];0.87[CHB][hapmap];0.81[EUR][1000 genomes]
rs12693384	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12693385	0.82[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap]
rs13021843	0.81[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs13026742	0.86[JPT][hapmap]
rs13393273	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13405270	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1427150	1.00[JPT][hapmap]
rs1480478	0.82[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.83[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs17430600	1.00[CEU][hapmap];1.00[CHB][hapmap];0.82[JPT][hapmap]
rs17508595	1.00[JPT][hapmap]
rs2054548	0.81[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs2054549	0.92[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs2369593	0.90[YRI][hapmap]
rs2369595	0.85[JPT][hapmap]
rs359882	0.82[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap];0.85[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs359884	0.82[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs359885	0.82[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs359886	0.82[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.85[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs359891	0.95[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs359895	1.00[CHB][hapmap];0.90[YRI][hapmap];0.87[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs403115	0.85[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs430040	0.90[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs435822	0.96[CEU][hapmap];1.00[CHB][hapmap];0.90[YRI][hapmap];0.91[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs55764167	0.86[ASN][1000 genomes]
rs6434094	0.85[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs6434095	0.82[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs6434096	0.82[CHB][hapmap];1.00[JPT][hapmap];0.83[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs6728764	0.93[CHB][hapmap];0.85[JPT][hapmap];0.87[ASN][1000 genomes]
rs73041394	0.83[ASN][1000 genomes]
rs73043234	0.83[ASN][1000 genomes]
rs7564347	0.93[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs7608194	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7608284	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs899847	0.82[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs9288106	1.00[JPT][hapmap]

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	nsv532412	chr2:185347334-186108701	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	esv1818452	chr2:185428946-185503154	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:185495000-185497400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
2	chr2:185497200-185500400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr2:185497200-185502600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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