Variant report

Variant	rs10064657
Chromosome Location	chr5:148129958-148129959
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:148121456..148124222-chr5:148128442..148130546,2	K562	blood:

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10066472	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10072157	0.81[AFR][1000 genomes]
rs10075525	0.93[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10078988	0.81[AFR][1000 genomes]
rs10079055	0.81[AFR][1000 genomes]
rs11952301	1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11953048	0.80[AFR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13358515	0.90[AFR][1000 genomes]
rs13358560	1.00[ASN][1000 genomes]
rs6580570	1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6580571	0.80[AFR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6580572	0.83[AFR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6580573	0.80[AFR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6580575	0.80[AFR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6580576	0.80[AFR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6580577	0.83[AFR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6864773	0.81[AFR][1000 genomes]
rs6877622	0.80[AFR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6885180	0.83[AFR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6891709	0.90[AFR][1000 genomes]
rs6898652	0.83[AFR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7700539	0.80[AFR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7719592	0.80[AFR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7738035	0.80[AFR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][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	nsv883021	chr5:148060817-148182123	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:148119600-148135000	Weak transcription	Right Atrium	heart
2	chr5:148125400-148131200	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr5:148125600-148131600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr5:148125800-148130800	Enhancers	Primary hematopoietic stem cells	blood
5	chr5:148127400-148130200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr5:148127600-148131600	Enhancers	Primary hematopoietic stem cells short term culture	blood
7	chr5:148128800-148130200	Weak transcription	Fetal Heart	heart
8	chr5:148129000-148130200	Weak transcription	Primary B cells from cord blood	blood
9	chr5:148129200-148131800	Enhancers	Primary neutrophils fromperipheralblood	blood
10	chr5:148129400-148130800	Enhancers	Monocytes-CD14+_RO01746	blood
11	chr5:148129800-148130600	Enhancers	Adipose Nuclei	Adipose

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