Variant report

Variant	rs72947961
Chromosome Location	chr11:84944706-84944707
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 130 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:126)

rs_ID	r²[population]
rs10501589	0.93[ASN][1000 genomes]
rs10501592	0.93[ASN][1000 genomes]
rs11821513	0.96[ASN][1000 genomes]
rs11822362	0.96[ASN][1000 genomes]
rs11823732	0.94[ASN][1000 genomes]
rs11823978	0.98[ASN][1000 genomes]
rs11825901	0.98[ASN][1000 genomes]
rs11827372	0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12281150	0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12788992	0.93[ASN][1000 genomes]
rs1602992	0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17148016	0.93[ASN][1000 genomes]
rs17148028	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17148049	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17148061	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17148063	0.94[ASN][1000 genomes]
rs17148067	0.94[ASN][1000 genomes]
rs17148070	0.94[ASN][1000 genomes]
rs17148078	0.93[ASN][1000 genomes]
rs17148086	0.98[ASN][1000 genomes]
rs17148090	0.93[ASN][1000 genomes]
rs17159864	0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17207843	0.93[ASN][1000 genomes]
rs17207864	0.94[ASN][1000 genomes]
rs17208108	0.94[ASN][1000 genomes]
rs17208150	0.93[ASN][1000 genomes]
rs17208171	0.94[ASN][1000 genomes]
rs17208192	0.94[ASN][1000 genomes]
rs17810172	0.81[ASN][1000 genomes]
rs17810291	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17810357	0.94[ASN][1000 genomes]
rs17810405	0.94[ASN][1000 genomes]
rs17810429	0.94[ASN][1000 genomes]
rs17810490	0.93[ASN][1000 genomes]
rs17810611	0.80[ASN][1000 genomes]
rs1914371	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1914372	0.94[ASN][1000 genomes]
rs2032410	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2036782	0.86[ASN][1000 genomes]
rs2056182	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2088015	0.93[ASN][1000 genomes]
rs2088016	0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2088017	0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2213116	0.91[ASN][1000 genomes]
rs3941173	0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs56306275	0.91[ASN][1000 genomes]
rs57104960	0.91[ASN][1000 genomes]
rs57671189	0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs58028528	0.93[ASN][1000 genomes]
rs58117031	0.80[ASN][1000 genomes]
rs58464081	0.93[ASN][1000 genomes]
rs58515356	0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs58756447	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59464672	0.80[ASN][1000 genomes]
rs59583891	0.98[ASN][1000 genomes]
rs59713586	0.80[ASN][1000 genomes]
rs59851854	0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs59869002	0.91[ASN][1000 genomes]
rs60030322	0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs60284674	0.81[ASN][1000 genomes]
rs60360244	0.94[ASN][1000 genomes]
rs60383907	0.93[ASN][1000 genomes]
rs61368496	0.93[ASN][1000 genomes]
rs61697848	0.89[ASN][1000 genomes]
rs6592235	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6592236	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7110155	0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7117010	0.86[ASN][1000 genomes]
rs72945906	0.93[ASN][1000 genomes]
rs72945910	0.93[ASN][1000 genomes]
rs72945914	0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72945917	0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72945919	0.93[ASN][1000 genomes]
rs72945920	0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72945921	0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72945944	0.94[ASN][1000 genomes]
rs72945948	0.94[ASN][1000 genomes]
rs72945956	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72945965	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72947963	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72947971	0.94[ASN][1000 genomes]
rs72947974	0.94[ASN][1000 genomes]
rs72947975	0.94[ASN][1000 genomes]
rs72947981	0.94[ASN][1000 genomes]
rs72947999	0.94[ASN][1000 genomes]
rs72950104	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72950107	0.93[ASN][1000 genomes]
rs72950109	0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72950128	0.93[ASN][1000 genomes]
rs72950129	0.93[ASN][1000 genomes]
rs72950131	0.93[ASN][1000 genomes]
rs72950137	0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72950141	0.91[ASN][1000 genomes]
rs72950152	0.93[ASN][1000 genomes]
rs72950153	0.93[ASN][1000 genomes]
rs72950156	0.93[ASN][1000 genomes]
rs72950157	0.93[ASN][1000 genomes]
rs72950158	0.93[ASN][1000 genomes]
rs72950161	0.93[ASN][1000 genomes]
rs72950165	0.93[ASN][1000 genomes]
rs72950167	0.93[ASN][1000 genomes]
rs72950168	0.93[ASN][1000 genomes]
rs72950169	0.93[ASN][1000 genomes]
rs72950175	0.93[ASN][1000 genomes]
rs72950176	0.93[ASN][1000 genomes]
rs72950181	0.93[ASN][1000 genomes]
rs72950182	0.93[ASN][1000 genomes]
rs72950186	0.91[ASN][1000 genomes]
rs72951917	0.91[ASN][1000 genomes]
rs72951920	0.80[ASN][1000 genomes]
rs72961528	0.93[ASN][1000 genomes]
rs72961539	0.96[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72961540	0.89[ASN][1000 genomes]
rs72961550	0.93[ASN][1000 genomes]
rs72961552	0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72961553	0.93[ASN][1000 genomes]
rs72961554	0.89[AMR][1000 genomes];0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72961555	0.93[ASN][1000 genomes]
rs72961557	0.93[ASN][1000 genomes]
rs72961558	0.93[ASN][1000 genomes]
rs72961562	0.93[ASN][1000 genomes]
rs72961567	0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72961570	0.93[ASN][1000 genomes]
rs7924587	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7940610	0.93[ASN][1000 genomes]
rs7947098	0.89[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	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	nsv898042	chr11:84877221-84965437	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
3	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
4	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

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:84944200-84945000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr11:84944600-84947200	Weak transcription	HUES48 Cell Line	embryonic stem cell

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