Variant report

Variant	rs59869002
Chromosome Location	chr11:85052357-85052358
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 134 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:129)

rs_ID	r²[population]
rs10501589	0.98[ASN][1000 genomes]
rs10501592	0.98[ASN][1000 genomes]
rs11821513	0.94[ASN][1000 genomes]
rs11822362	0.94[ASN][1000 genomes]
rs11823732	0.96[ASN][1000 genomes]
rs11823978	0.93[ASN][1000 genomes]
rs11825901	0.93[ASN][1000 genomes]
rs11827372	0.93[ASN][1000 genomes]
rs12788992	0.98[ASN][1000 genomes]
rs1602992	0.89[ASN][1000 genomes]
rs17148016	0.98[ASN][1000 genomes]
rs17148028	0.84[ASN][1000 genomes]
rs17148049	0.91[ASN][1000 genomes]
rs17148061	0.91[ASN][1000 genomes]
rs17148063	0.96[ASN][1000 genomes]
rs17148067	0.96[ASN][1000 genomes]
rs17148070	0.96[ASN][1000 genomes]
rs17148078	0.98[ASN][1000 genomes]
rs17148086	0.93[ASN][1000 genomes]
rs17148090	0.98[ASN][1000 genomes]
rs17159864	0.94[ASN][1000 genomes]
rs17207843	0.98[ASN][1000 genomes]
rs17207864	0.96[ASN][1000 genomes]
rs17208108	0.96[ASN][1000 genomes]
rs17208150	0.94[ASN][1000 genomes]
rs17208171	0.96[ASN][1000 genomes]
rs17208192	0.96[ASN][1000 genomes]
rs17810172	0.83[ASN][1000 genomes]
rs17810291	0.91[ASN][1000 genomes]
rs17810357	0.96[ASN][1000 genomes]
rs17810405	0.96[ASN][1000 genomes]
rs17810429	0.96[ASN][1000 genomes]
rs17810490	0.98[ASN][1000 genomes]
rs17810611	0.89[ASN][1000 genomes]
rs1914371	0.91[ASN][1000 genomes]
rs1914372	0.96[ASN][1000 genomes]
rs2032410	0.91[ASN][1000 genomes]
rs2036782	0.84[ASN][1000 genomes]
rs2056182	0.91[ASN][1000 genomes]
rs2088015	0.98[ASN][1000 genomes]
rs2088016	0.89[ASN][1000 genomes]
rs2088017	0.89[ASN][1000 genomes]
rs2213116	1.00[ASN][1000 genomes]
rs3941173	0.89[ASN][1000 genomes]
rs56306275	0.92[ASN][1000 genomes]
rs57104960	1.00[ASN][1000 genomes]
rs57494426	0.81[ASN][1000 genomes]
rs57671189	0.89[ASN][1000 genomes]
rs58028528	0.98[ASN][1000 genomes]
rs58117031	0.89[ASN][1000 genomes]
rs58464081	0.98[ASN][1000 genomes]
rs58515356	0.88[ASN][1000 genomes]
rs58756447	0.91[ASN][1000 genomes]
rs59464672	0.89[ASN][1000 genomes]
rs59583891	0.93[ASN][1000 genomes]
rs59713586	0.89[ASN][1000 genomes]
rs59851854	0.89[ASN][1000 genomes]
rs60030322	0.89[ASN][1000 genomes]
rs60284674	0.83[ASN][1000 genomes]
rs60360244	0.96[ASN][1000 genomes]
rs60383907	0.98[ASN][1000 genomes]
rs61368496	0.98[ASN][1000 genomes]
rs61697848	0.94[ASN][1000 genomes]
rs6592235	0.93[ASN][1000 genomes]
rs6592236	0.93[ASN][1000 genomes]
rs7110155	0.89[ASN][1000 genomes]
rs7117010	0.84[ASN][1000 genomes]
rs72945906	0.98[ASN][1000 genomes]
rs72945910	0.98[ASN][1000 genomes]
rs72945914	0.89[ASN][1000 genomes]
rs72945917	0.89[ASN][1000 genomes]
rs72945919	0.98[ASN][1000 genomes]
rs72945920	0.89[ASN][1000 genomes]
rs72945921	0.89[ASN][1000 genomes]
rs72945944	0.96[ASN][1000 genomes]
rs72945948	0.96[ASN][1000 genomes]
rs72945956	0.91[ASN][1000 genomes]
rs72945965	0.91[ASN][1000 genomes]
rs72947961	0.91[ASN][1000 genomes]
rs72947963	0.91[ASN][1000 genomes]
rs72947971	0.96[ASN][1000 genomes]
rs72947974	0.96[ASN][1000 genomes]
rs72947975	0.96[ASN][1000 genomes]
rs72947981	0.96[ASN][1000 genomes]
rs72947999	0.96[ASN][1000 genomes]
rs72950104	0.91[ASN][1000 genomes]
rs72950107	0.98[ASN][1000 genomes]
rs72950109	0.93[ASN][1000 genomes]
rs72950128	0.98[ASN][1000 genomes]
rs72950129	0.98[ASN][1000 genomes]
rs72950131	0.98[ASN][1000 genomes]
rs72950137	0.93[ASN][1000 genomes]
rs72950141	0.96[ASN][1000 genomes]
rs72950152	0.98[ASN][1000 genomes]
rs72950153	0.98[ASN][1000 genomes]
rs72950156	0.98[ASN][1000 genomes]
rs72950157	0.98[ASN][1000 genomes]
rs72950158	0.98[ASN][1000 genomes]
rs72950161	0.98[ASN][1000 genomes]
rs72950165	0.98[ASN][1000 genomes]
rs72950167	0.98[ASN][1000 genomes]
rs72950168	0.98[ASN][1000 genomes]
rs72950169	0.98[ASN][1000 genomes]
rs72950175	0.98[ASN][1000 genomes]
rs72950176	0.98[ASN][1000 genomes]
rs72950181	0.98[ASN][1000 genomes]
rs72950182	0.98[ASN][1000 genomes]
rs72950186	1.00[ASN][1000 genomes]
rs72951917	1.00[ASN][1000 genomes]
rs72951920	0.89[ASN][1000 genomes]
rs72951948	0.85[ASN][1000 genomes]
rs72951958	0.81[ASN][1000 genomes]
rs72951961	0.81[ASN][1000 genomes]
rs72961528	0.98[ASN][1000 genomes]
rs72961539	0.93[ASN][1000 genomes]
rs72961540	0.94[ASN][1000 genomes]
rs72961550	0.98[ASN][1000 genomes]
rs72961552	0.89[ASN][1000 genomes]
rs72961553	0.98[ASN][1000 genomes]
rs72961554	0.93[ASN][1000 genomes]
rs72961555	0.98[ASN][1000 genomes]
rs72961557	0.98[ASN][1000 genomes]
rs72961558	0.98[ASN][1000 genomes]
rs72961562	0.98[ASN][1000 genomes]
rs72961567	0.89[ASN][1000 genomes]
rs72961570	0.98[ASN][1000 genomes]
rs7924587	0.93[ASN][1000 genomes]
rs7940610	0.91[ASN][1000 genomes]
rs7947098	0.98[ASN][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	nsv1044370	chr11:84748993-85293233	Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
2	nsv898043	chr11:84895033-85148689	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv898044	chr11:84895033-85220773	ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
4	nsv1051155	chr11:85006564-85721261	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
5	nsv541110	chr11:85006564-85721261	Enhancers Strong transcription Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 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	chr11:85049600-85059400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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