Variant report

Variant	rs35235479
Chromosome Location	chr10:94527160-94527161
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:94518763..94521506-chr10:94525236..94529562,3	K562	blood:
2	chr10:94519112..94521506-chr10:94526689..94529605,3	K562	blood:

Extended variants
information (count: 46 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11187161	1.00[ASN][1000 genomes]
rs11187162	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11187164	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11187165	0.82[EUR][1000 genomes]
rs11187166	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11187167	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11187169	1.00[ASN][1000 genomes]
rs11187170	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11187171	0.82[EUR][1000 genomes]
rs11187173	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11187179	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12261163	0.84[ASN][1000 genomes]
rs12355562	0.94[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12358931	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12763565	1.00[ASN][1000 genomes]
rs12763786	1.00[ASN][1000 genomes]
rs12764758	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12765131	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12766137	0.92[ASN][1000 genomes]
rs12779884	1.00[ASN][1000 genomes]
rs12779990	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12780621	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12784232	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2488056	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2488066	0.92[ASN][1000 genomes]
rs2497351	1.00[ASN][1000 genomes]
rs34269987	0.97[AFR][1000 genomes];0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34478558	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34566437	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs34636435	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34664889	1.00[ASN][1000 genomes]
rs35001517	1.00[ASN][1000 genomes]
rs35039517	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs36016244	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36082564	1.00[ASN][1000 genomes]
rs55851824	1.00[ASN][1000 genomes]
rs55951294	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56026908	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61862826	1.00[ASN][1000 genomes]
rs6583840	1.00[ASN][1000 genomes]
rs67412949	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7091916	0.82[EUR][1000 genomes]
rs71480841	1.00[ASN][1000 genomes]
rs7896131	1.00[ASN][1000 genomes]
rs882136	0.81[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	esv3446249	chr10:94374508-94549394	Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Weak transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:94526800-94527200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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