Variant report

Variant	rs72961554
Chromosome Location	chr11:84863696-84863697
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 125 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:121)

rs_ID	r²[population]
rs10501589	0.93[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs10501592	0.91[ASN][1000 genomes]
rs11821513	0.98[ASN][1000 genomes]
rs11822362	0.98[ASN][1000 genomes]
rs11823732	0.93[ASN][1000 genomes]
rs11823978	0.96[ASN][1000 genomes]
rs11825901	0.96[ASN][1000 genomes]
rs11827372	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12281150	0.84[ASN][1000 genomes]
rs12788992	0.91[ASN][1000 genomes]
rs1602992	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17148016	0.90[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs17148028	0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17148049	0.90[AMR][1000 genomes];0.80[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17148061	0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17148063	0.93[ASN][1000 genomes]
rs17148067	0.93[ASN][1000 genomes]
rs17148070	0.93[ASN][1000 genomes]
rs17148078	0.91[ASN][1000 genomes]
rs17148086	0.96[ASN][1000 genomes]
rs17148090	0.91[ASN][1000 genomes]
rs17159864	0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs17207843	0.86[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs17207864	0.93[ASN][1000 genomes]
rs17208108	0.93[ASN][1000 genomes]
rs17208150	0.91[ASN][1000 genomes]
rs17208171	0.93[ASN][1000 genomes]
rs17208192	0.93[ASN][1000 genomes]
rs17810291	0.89[AMR][1000 genomes];0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17810357	0.93[ASN][1000 genomes]
rs17810405	0.93[ASN][1000 genomes]
rs17810429	0.93[ASN][1000 genomes]
rs17810490	0.91[ASN][1000 genomes]
rs1914371	0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1914372	0.93[ASN][1000 genomes]
rs2032410	0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2036782	0.87[ASN][1000 genomes]
rs2056182	0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2088015	0.97[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs2088016	0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2088017	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2213116	0.93[ASN][1000 genomes]
rs3941173	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs56306275	0.89[ASN][1000 genomes]
rs57104960	0.93[ASN][1000 genomes]
rs57671189	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs58028528	0.94[ASN][1000 genomes]
rs58464081	0.91[ASN][1000 genomes]
rs58515356	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs58756447	0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs59464672	0.82[ASN][1000 genomes]
rs59583891	0.96[ASN][1000 genomes]
rs59713586	0.82[ASN][1000 genomes]
rs59851854	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs59869002	0.93[ASN][1000 genomes]
rs60030322	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs60360244	0.93[ASN][1000 genomes]
rs60383907	0.85[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs61368496	0.94[ASN][1000 genomes]
rs61697848	0.87[ASN][1000 genomes]
rs6592235	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6592236	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7110155	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72945906	0.94[ASN][1000 genomes]
rs72945910	0.94[ASN][1000 genomes]
rs72945914	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72945917	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72945919	0.94[ASN][1000 genomes]
rs72945920	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72945921	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72945944	0.93[ASN][1000 genomes]
rs72945948	0.93[ASN][1000 genomes]
rs72945956	0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72945965	0.98[ASN][1000 genomes]
rs72947961	0.89[AMR][1000 genomes];0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72947963	0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72947971	0.93[ASN][1000 genomes]
rs72947974	0.93[ASN][1000 genomes]
rs72947975	0.93[ASN][1000 genomes]
rs72947981	0.93[ASN][1000 genomes]
rs72947999	0.93[ASN][1000 genomes]
rs72950104	0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72950107	0.91[ASN][1000 genomes]
rs72950109	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72950128	0.91[ASN][1000 genomes]
rs72950129	0.91[ASN][1000 genomes]
rs72950131	0.91[ASN][1000 genomes]
rs72950137	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72950141	0.89[ASN][1000 genomes]
rs72950152	0.91[ASN][1000 genomes]
rs72950153	0.91[ASN][1000 genomes]
rs72950156	0.91[ASN][1000 genomes]
rs72950157	0.91[ASN][1000 genomes]
rs72950158	0.91[ASN][1000 genomes]
rs72950161	0.91[ASN][1000 genomes]
rs72950165	0.91[ASN][1000 genomes]
rs72950167	0.91[ASN][1000 genomes]
rs72950168	0.91[ASN][1000 genomes]
rs72950169	0.91[ASN][1000 genomes]
rs72950175	0.91[ASN][1000 genomes]
rs72950176	0.91[ASN][1000 genomes]
rs72950181	0.91[ASN][1000 genomes]
rs72950182	0.91[ASN][1000 genomes]
rs72950186	0.93[ASN][1000 genomes]
rs72951917	0.93[ASN][1000 genomes]
rs72951920	0.82[ASN][1000 genomes]
rs72961528	0.94[ASN][1000 genomes]
rs72961539	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72961540	0.91[ASN][1000 genomes]
rs72961550	0.94[ASN][1000 genomes]
rs72961552	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72961553	0.95[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs72961555	0.94[ASN][1000 genomes]
rs72961557	0.88[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs72961558	0.88[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs72961562	0.94[ASN][1000 genomes]
rs72961567	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72961570	0.94[ASN][1000 genomes]
rs7924587	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7940610	0.95[ASN][1000 genomes]
rs7947098	0.91[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	nsv1040393	chr11:84708402-84866594	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv527535	chr11:84724795-84895033	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv528491	chr11:84724795-84895033	Weak transcription Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	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

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:84861400-84865200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links