Variant report

Variant	rs73547611
Chromosome Location	chr6:133218971-133218972
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:133218271..133221102-chr6:133233922..133236675,2	K562	blood:

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

rSNPs within LD-proxies of this variant (count:60)

rs_ID	r²[population]
rs1122175	0.81[ASN][1000 genomes]
rs11965927	0.81[ASN][1000 genomes]
rs34688576	0.81[ASN][1000 genomes]
rs34934410	0.81[ASN][1000 genomes]
rs35148730	0.81[ASN][1000 genomes]
rs3736725	0.81[ASN][1000 genomes]
rs3756971	0.81[ASN][1000 genomes]
rs41286184	0.81[ASN][1000 genomes]
rs56908272	0.81[ASN][1000 genomes]
rs57176306	0.91[ASN][1000 genomes]
rs58949949	1.00[ASN][1000 genomes]
rs59357932	0.91[ASN][1000 genomes]
rs59716502	0.81[ASN][1000 genomes]
rs59718818	0.81[ASN][1000 genomes]
rs60133731	0.81[ASN][1000 genomes]
rs60177375	0.91[ASN][1000 genomes]
rs60631157	0.81[ASN][1000 genomes]
rs61310652	0.81[ASN][1000 genomes]
rs6569851	0.81[ASN][1000 genomes]
rs6569852	0.81[ASN][1000 genomes]
rs6905784	0.81[ASN][1000 genomes]
rs6911773	0.81[ASN][1000 genomes]
rs6924403	0.91[ASN][1000 genomes]
rs6926101	0.81[ASN][1000 genomes]
rs6927991	0.81[ASN][1000 genomes]
rs6928237	0.81[ASN][1000 genomes]
rs6928933	0.81[ASN][1000 genomes]
rs6930549	0.81[ASN][1000 genomes]
rs6930703	0.81[ASN][1000 genomes]
rs6934155	0.81[ASN][1000 genomes]
rs6934190	0.81[ASN][1000 genomes]
rs73550455	0.81[ASN][1000 genomes]
rs73554461	0.91[ASN][1000 genomes]
rs73558375	0.91[ASN][1000 genomes]
rs73558378	0.91[ASN][1000 genomes]
rs73558387	0.91[ASN][1000 genomes]
rs7738256	0.81[ASN][1000 genomes]
rs7738569	0.81[ASN][1000 genomes]
rs7747544	0.81[ASN][1000 genomes]
rs7748090	0.91[ASN][1000 genomes]
rs7753595	0.81[ASN][1000 genomes]
rs7759524	0.81[ASN][1000 genomes]
rs7761207	0.81[ASN][1000 genomes]
rs7762248	0.81[ASN][1000 genomes]
rs7769354	0.91[ASN][1000 genomes]
rs7775241	0.81[ASN][1000 genomes]
rs9321369	0.81[ASN][1000 genomes]
rs9321370	0.81[ASN][1000 genomes]
rs9321375	0.91[ASN][1000 genomes]
rs9483501	0.81[ASN][1000 genomes]
rs9483502	0.81[ASN][1000 genomes]
rs9493434	0.81[ASN][1000 genomes]
rs9493440	0.81[ASN][1000 genomes]
rs9493441	0.81[ASN][1000 genomes]
rs9493447	0.81[ASN][1000 genomes]
rs9493449	0.81[ASN][1000 genomes]
rs9493455	0.91[ASN][1000 genomes]
rs9493457	0.91[ASN][1000 genomes]
rs9766095	0.81[ASN][1000 genomes]
rs9767075	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532069	chr6:132776411-133462292	Active TSS Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
2	nsv1015742	chr6:132933666-133285852	Active TSS Flanking Active TSS Enhancers Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	71 gene(s)	inside rSNPs	diseases
3	nsv869855	chr6:133190265-133244259	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 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	chr6:133218800-133219400	Enhancers	Fetal Muscle Trunk	muscle

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