Variant report

Variant	rs58956072
Chromosome Location	chr4:175278065-175278066
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	chr4:175277556..175279141-chr4:175280791..175283093,2	K562	blood:
2	chr4:175274108..175277040-chr4:175277459..175280038,2	K562	blood:

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10446854	1.00[ASN][1000 genomes]
rs11939414	0.82[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs13101256	1.00[ASN][1000 genomes]
rs13125731	1.00[ASN][1000 genomes]
rs13151156	1.00[ASN][1000 genomes]
rs34066344	0.88[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs34274380	0.84[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs34369193	0.87[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs34698083	0.82[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs34765808	0.88[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs35377027	0.88[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs35473266	1.00[ASN][1000 genomes]
rs35567270	0.88[AMR][1000 genomes]
rs4280712	0.87[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs4293767	0.87[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs4306937	0.88[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4408938	0.87[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs4408939	0.87[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs4428259	0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4447835	0.88[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4452408	0.88[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4458430	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4469047	1.00[ASN][1000 genomes]
rs4695777	0.88[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4695926	0.84[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs4695927	0.88[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs4695928	0.87[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs4695930	1.00[ASN][1000 genomes]
rs4695931	1.00[ASN][1000 genomes]
rs56041548	1.00[ASN][1000 genomes]
rs58895800	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs67509565	0.82[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs6812756	0.83[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs6814901	0.88[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6817902	0.87[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs6831848	0.88[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6855058	0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6855451	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72702283	1.00[ASN][1000 genomes]
rs7656670	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1016910	chr4:174952788-175349057	Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
2	nsv537363	chr4:174952788-175349057	Active TSS Bivalent Enhancer Weak transcription Enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
3	nsv596234	chr4:175053051-175361437	Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
4	nsv869116	chr4:175231090-175801761	Flanking Active TSS Enhancers Genic enhancers Weak transcription Bivalent/Poised TSS Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 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	chr4:175274200-175279600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr4:175274400-175279600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr4:175277400-175278400	Weak transcription	Left Ventricle	heart

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