Variant report

Variant	rs1508818
Chromosome Location	chr5:41888912-41888913
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr5:41877897..41883547-chr5:41886069..41890189,5	K562	blood:
2	chr5:41883917..41886978-chr5:41887352..41891327,3	K562	blood:
3	chr5:41888696..41891636-chr5:41903248..41905861,3	MCF-7	breast:
4	chr5:41882384..41891851-chr5:41900562..41907560,15	K562	blood:
5	chr5:41887319..41889409-chr5:41922980..41925910,2	K562	blood:

Variant related genes	Relation type
ENSG00000151876	Chromatin interaction
ENSG00000205765	Chromatin interaction

Extended variants
information (count: 102 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:97)

rs_ID	r²[population]
rs10941559	0.89[CEU][hapmap];0.92[EUR][1000 genomes]
rs11738517	0.83[EUR][1000 genomes]
rs11739106	0.91[EUR][1000 genomes]
rs11739257	0.89[CEU][hapmap];0.91[EUR][1000 genomes]
rs11740524	0.92[EUR][1000 genomes]
rs11740946	0.89[EUR][1000 genomes]
rs11742249	0.98[EUR][1000 genomes]
rs11744279	0.88[CEU][hapmap];0.89[EUR][1000 genomes]
rs11744516	0.89[EUR][1000 genomes]
rs11744623	0.92[EUR][1000 genomes]
rs11746511	0.91[EUR][1000 genomes]
rs11747881	0.88[CEU][hapmap];0.89[EUR][1000 genomes]
rs11747921	0.92[CEU][hapmap];0.89[EUR][1000 genomes]
rs11749008	0.87[EUR][1000 genomes]
rs11750607	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11750760	0.80[CEU][hapmap];0.89[EUR][1000 genomes]
rs11750790	0.89[EUR][1000 genomes]
rs13153468	0.88[CEU][hapmap];0.89[EUR][1000 genomes]
rs13153837	0.91[EUR][1000 genomes]
rs13156367	0.98[EUR][1000 genomes]
rs13162040	0.89[EUR][1000 genomes]
rs13163137	0.89[EUR][1000 genomes]
rs13164201	0.91[EUR][1000 genomes]
rs13165731	0.90[EUR][1000 genomes]
rs13167578	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs13168035	0.89[EUR][1000 genomes]
rs13169285	0.82[EUR][1000 genomes]
rs13169977	0.89[EUR][1000 genomes]
rs13170096	0.99[EUR][1000 genomes]
rs13176368	0.89[EUR][1000 genomes]
rs13177937	0.89[EUR][1000 genomes]
rs13179852	0.89[EUR][1000 genomes]
rs13180405	1.00[CEU][hapmap];0.99[EUR][1000 genomes]
rs13182336	0.89[EUR][1000 genomes]
rs13185973	0.88[CEU][hapmap];0.89[EUR][1000 genomes]
rs13189403	0.84[EUR][1000 genomes]
rs1345781	0.84[EUR][1000 genomes]
rs1508815	0.89[EUR][1000 genomes]
rs16871955	0.89[EUR][1000 genomes]
rs16871972	0.91[EUR][1000 genomes]
rs16900142	0.89[CEU][hapmap];0.92[EUR][1000 genomes]
rs1876653	0.92[EUR][1000 genomes]
rs1876654	0.85[CEU][hapmap];0.90[EUR][1000 genomes]
rs33967331	0.89[EUR][1000 genomes]
rs34048302	0.82[EUR][1000 genomes]
rs34071445	0.89[EUR][1000 genomes]
rs34329864	0.89[EUR][1000 genomes]
rs34339137	0.89[EUR][1000 genomes]
rs34369972	0.89[EUR][1000 genomes]
rs34412181	0.87[EUR][1000 genomes]
rs34500930	0.89[EUR][1000 genomes]
rs34569700	0.89[EUR][1000 genomes]
rs34625465	0.89[EUR][1000 genomes]
rs34663371	0.89[EUR][1000 genomes]
rs34841703	0.89[EUR][1000 genomes]
rs34873414	0.89[EUR][1000 genomes]
rs35077044	0.88[CEU][hapmap];0.89[EUR][1000 genomes]
rs35244816	0.97[EUR][1000 genomes]
rs35252930	0.89[EUR][1000 genomes]
rs35343042	0.88[EUR][1000 genomes]
rs35613904	0.92[EUR][1000 genomes]
rs35748945	1.00[EUR][1000 genomes]
rs35764180	0.88[EUR][1000 genomes]
rs35861205	0.89[EUR][1000 genomes]
rs36005620	0.89[EUR][1000 genomes]
rs36009913	0.98[EUR][1000 genomes]
rs36113900	0.89[EUR][1000 genomes]
rs3926618	0.89[EUR][1000 genomes]
rs4957430	0.88[CEU][hapmap];0.91[EUR][1000 genomes]
rs55817686	0.88[EUR][1000 genomes]
rs56017638	0.89[EUR][1000 genomes]
rs60209308	0.89[EUR][1000 genomes]
rs62360542	0.83[EUR][1000 genomes]
rs66820325	0.91[EUR][1000 genomes]
rs67114999	0.89[EUR][1000 genomes]
rs67206815	0.88[EUR][1000 genomes]
rs67715253	0.88[EUR][1000 genomes]
rs67869805	0.91[EUR][1000 genomes]
rs6865448	0.89[EUR][1000 genomes]
rs6866549	0.89[EUR][1000 genomes]
rs6879341	0.88[CEU][hapmap];0.89[EUR][1000 genomes]
rs6881206	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6881873	0.91[EUR][1000 genomes]
rs6883144	0.89[EUR][1000 genomes]
rs6888816	0.89[EUR][1000 genomes]
rs6889217	0.89[CEU][hapmap];0.89[EUR][1000 genomes]
rs72746918	0.88[EUR][1000 genomes]
rs72746919	0.88[EUR][1000 genomes]
rs72746957	0.89[EUR][1000 genomes]
rs7709500	0.88[CEU][hapmap];0.89[EUR][1000 genomes]
rs7712911	0.89[CEU][hapmap];0.89[EUR][1000 genomes]
rs7721136	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7724934	0.88[EUR][1000 genomes]
rs7725264	0.94[CEU][hapmap];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs951883	0.89[EUR][1000 genomes]
rs964267	0.89[EUR][1000 genomes]
rs9687619	0.88[CEU][hapmap];0.92[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830271	chr5:41716527-41895710	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
2	esv2762518	chr5:41780210-41935113	Flanking Active TSS Weak transcription Enhancers Strong transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	108 gene(s)	inside rSNPs	diseases
3	nsv830272	chr5:41833365-41986167	Strong transcription Enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	111 gene(s)	inside rSNPs	diseases
4	nsv830273	chr5:41867296-42066070	Flanking Active TSS Active TSS Genic enhancers Weak transcription Bivalent Enhancer Enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	111 gene(s)	inside rSNPs	diseases
5	nsv933208	chr5:41879946-42876624	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	112 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs1508818	OXCT1	Cis_1M	lymphoblastoid	RTeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:41888600-41889800	Weak transcription	K562	blood

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