Variant report

Variant	rs60794509
Chromosome Location	chr6:24769093-24769094
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	chr6:24765911..24769341-chr6:24775043..24776588,3	K562	blood:
2	chr6:24765911..24769341-chr6:24773986..24776544,3	K562	blood:

Variant related genes	Relation type
ENSG00000112312	Chromatin interaction

Extended variants
information (count: 89 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:85)

rs_ID	r²[population]
rs1002649	0.81[AFR][1000 genomes]
rs10946726	0.95[ASN][1000 genomes]
rs11968288	0.95[ASN][1000 genomes]
rs12183400	0.81[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs16889670	0.95[ASN][1000 genomes]
rs16889688	0.95[ASN][1000 genomes]
rs2295735	0.95[ASN][1000 genomes]
rs2307306	0.95[ASN][1000 genomes]
rs2307307	0.95[ASN][1000 genomes]
rs28561768	0.95[ASN][1000 genomes]
rs3756809	0.95[ASN][1000 genomes]
rs3756810	0.95[ASN][1000 genomes]
rs3756811	0.95[ASN][1000 genomes]
rs3756812	0.95[ASN][1000 genomes]
rs3813682	0.95[ASN][1000 genomes]
rs56208026	0.95[ASN][1000 genomes]
rs58334728	0.95[ASN][1000 genomes]
rs58898420	0.95[ASN][1000 genomes]
rs59427770	0.95[ASN][1000 genomes]
rs59587218	0.95[ASN][1000 genomes]
rs59904886	0.95[ASN][1000 genomes]
rs6456634	0.95[ASN][1000 genomes]
rs6456635	0.95[ASN][1000 genomes]
rs6901466	0.81[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs6912564	0.95[ASN][1000 genomes]
rs6916816	0.95[ASN][1000 genomes]
rs6917565	0.95[ASN][1000 genomes]
rs6917813	0.95[ASN][1000 genomes]
rs6934938	0.81[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs6935339	0.80[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs6939757	0.95[ASN][1000 genomes]
rs6940028	0.81[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs73394570	0.95[ASN][1000 genomes]
rs73394572	0.95[ASN][1000 genomes]
rs73394575	0.95[ASN][1000 genomes]
rs73394577	0.95[ASN][1000 genomes]
rs73394578	0.95[ASN][1000 genomes]
rs73394591	0.81[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs73396404	0.95[ASN][1000 genomes]
rs73396407	0.95[ASN][1000 genomes]
rs73396430	0.95[ASN][1000 genomes]
rs73396439	0.95[ASN][1000 genomes]
rs73396453	0.95[ASN][1000 genomes]
rs7356832	0.95[ASN][1000 genomes]
rs7357034	0.95[ASN][1000 genomes]
rs73728683	0.82[ASN][1000 genomes]
rs7757501	0.83[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs7771372	0.95[ASN][1000 genomes]
rs7771462	0.95[ASN][1000 genomes]
rs7775042	0.83[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs9295632	0.95[ASN][1000 genomes]
rs9295634	0.95[ASN][1000 genomes]
rs9461060	0.82[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs9461061	0.81[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs9461062	0.81[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs9461063	0.81[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs9461064	0.81[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs9461065	0.81[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs9461067	0.95[ASN][1000 genomes]
rs9461068	0.95[ASN][1000 genomes]
rs9461069	0.95[ASN][1000 genomes]
rs9461071	0.95[ASN][1000 genomes]
rs9467284	0.95[ASN][1000 genomes]
rs9467285	0.95[ASN][1000 genomes]
rs9467286	0.95[ASN][1000 genomes]
rs9467288	0.95[ASN][1000 genomes]
rs9467289	0.95[ASN][1000 genomes]
rs9467290	0.81[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs9467291	0.81[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs9467292	0.81[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs9467293	0.95[ASN][1000 genomes]
rs9467294	0.81[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs9467295	0.81[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs9467296	0.95[ASN][1000 genomes]
rs9467297	0.95[ASN][1000 genomes]
rs9467303	0.95[ASN][1000 genomes]
rs9467304	0.95[ASN][1000 genomes]
rs9467305	0.95[ASN][1000 genomes]
rs9467309	0.95[ASN][1000 genomes]
rs9467311	0.95[ASN][1000 genomes]
rs9467312	0.95[ASN][1000 genomes]
rs9467316	0.95[ASN][1000 genomes]
rs9467317	0.95[ASN][1000 genomes]
rs9467318	0.95[ASN][1000 genomes]
rs9467319	0.95[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	nsv830609	chr6:24712086-24896647	Weak transcription Enhancers Strong transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	68 gene(s)	inside rSNPs	diseases
2	nsv428474	chr6:24714157-24797977	Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases
3	nsv1022966	chr6:24763776-25154212	Flanking Active TSS Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
4	nsv538160	chr6:24763776-25154212	Active TSS Strong transcription Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:24760400-24775000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr6:24764200-24771400	Weak transcription	K562	blood
3	chr6:24765400-24774400	Weak transcription	Fetal Intestine Small	intestine
4	chr6:24765800-24770600	Weak transcription	HepG2	liver
5	chr6:24767000-24774600	Weak transcription	Stomach Mucosa	stomach
6	chr6:24768800-24774200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr6:24769000-24771000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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