Variant report

Variant	rs17158586
Chromosome Location	chr7:103706997-103706998
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	chr7:103705230..103707654-chr7:103709368..103711788,2	K562	blood:

Extended variants
information (count: 63 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:62)

rs_ID	r²[population]
rs1019312	1.00[EUR][1000 genomes]
rs10234499	1.00[EUR][1000 genomes]
rs10235130	1.00[EUR][1000 genomes]
rs10235201	1.00[EUR][1000 genomes]
rs10241191	1.00[EUR][1000 genomes]
rs10242752	1.00[EUR][1000 genomes]
rs10250235	1.00[EUR][1000 genomes]
rs10251308	1.00[EUR][1000 genomes]
rs10251561	1.00[EUR][1000 genomes]
rs10255806	1.00[EUR][1000 genomes]
rs10256764	1.00[EUR][1000 genomes]
rs10258773	1.00[EUR][1000 genomes]
rs10262560	1.00[EUR][1000 genomes]
rs10262796	1.00[EUR][1000 genomes]
rs10262996	1.00[EUR][1000 genomes]
rs10263828	1.00[EUR][1000 genomes]
rs10266337	1.00[EUR][1000 genomes]
rs10267412	1.00[EUR][1000 genomes]
rs10267940	1.00[EUR][1000 genomes]
rs10268209	1.00[EUR][1000 genomes]
rs10270562	1.00[EUR][1000 genomes]
rs10271923	1.00[EUR][1000 genomes]
rs10275484	1.00[EUR][1000 genomes]
rs10278320	1.00[EUR][1000 genomes]
rs10279736	1.00[EUR][1000 genomes]
rs10281709	1.00[EUR][1000 genomes]
rs10282300	1.00[EUR][1000 genomes]
rs10487184	1.00[EUR][1000 genomes]
rs11489610	1.00[EUR][1000 genomes]
rs11972422	1.00[EUR][1000 genomes]
rs11979390	1.00[EUR][1000 genomes]
rs11979993	1.00[EUR][1000 genomes]
rs11980018	1.00[EUR][1000 genomes]
rs12112576	1.00[EUR][1000 genomes]
rs16873387	1.00[EUR][1000 genomes]
rs17159290	1.00[EUR][1000 genomes]
rs17159774	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2307409	1.00[EUR][1000 genomes]
rs2385134	1.00[EUR][1000 genomes]
rs28481813	1.00[EUR][1000 genomes]
rs28644319	1.00[EUR][1000 genomes]
rs28645598	1.00[EUR][1000 genomes]
rs28686914	1.00[EUR][1000 genomes]
rs28702500	1.00[EUR][1000 genomes]
rs28773535	1.00[EUR][1000 genomes]
rs58842751	1.00[EUR][1000 genomes]
rs59750244	1.00[EUR][1000 genomes]
rs6948021	1.00[EUR][1000 genomes]
rs6954109	1.00[EUR][1000 genomes]
rs6962621	1.00[EUR][1000 genomes]
rs6967711	1.00[EUR][1000 genomes]
rs6975642	1.00[EUR][1000 genomes]
rs73413894	1.00[EUR][1000 genomes]
rs73415730	1.00[EUR][1000 genomes]
rs73415786	1.00[EUR][1000 genomes]
rs73415801	1.00[EUR][1000 genomes]
rs73417705	1.00[EUR][1000 genomes]
rs73417718	1.00[EUR][1000 genomes]
rs7777446	1.00[EUR][1000 genomes]
rs7777906	1.00[EUR][1000 genomes]
rs7810496	1.00[EUR][1000 genomes]
rs9655777	1.00[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	nsv1018253	chr7:103669491-103731850	Enhancers Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:103706400-103708600	Enhancers	HepG2	liver

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