Variant report

Variant	rs4237605
Chromosome Location	chr11:101723234-101723235
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:101722375..101723959-chr11:101880701..101883311,2	MCF-7	breast:
2	chr11:101722861..101723655-chr11:101731427..101731999,2	MCF-7	breast:
3	chr11:101722724..101723429-chr11:101878801..101879552,2	MCF-7	breast:

Extended variants
information (count: 64 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs10501990	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10736621	0.90[AMR][1000 genomes]
rs10750622	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10791523	1.00[ASN][1000 genomes]
rs10791524	1.00[ASN][1000 genomes]
rs10791535	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10791539	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10791540	0.90[AMR][1000 genomes]
rs10895192	1.00[ASN][1000 genomes]
rs10895202	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1372415	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1441932	0.88[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1815903	0.91[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1815904	0.90[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1815905	0.91[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1939028	0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1939031	1.00[ASN][1000 genomes]
rs1939033	0.82[AMR][1000 genomes]
rs1939036	0.84[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs1939041	1.00[ASN][1000 genomes]
rs1939044	1.00[ASN][1000 genomes]
rs1939045	1.00[ASN][1000 genomes]
rs1939056	0.89[ASN][1000 genomes]
rs1939063	1.00[ASN][1000 genomes]
rs1939069	1.00[ASN][1000 genomes]
rs1939070	1.00[ASN][1000 genomes]
rs1939461	1.00[ASN][1000 genomes]
rs2000535	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2155064	1.00[ASN][1000 genomes]
rs2155066	1.00[ASN][1000 genomes]
rs2186611	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4084123	1.00[ASN][1000 genomes]
rs4237604	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4445600	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4576789	0.90[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4620692	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4754021	1.00[ASN][1000 genomes]
rs4754027	0.93[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4754031	0.91[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4754799	1.00[ASN][1000 genomes]
rs4754800	0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4754802	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4754805	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4754810	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4754812	0.90[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4754814	0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6590920	1.00[ASN][1000 genomes]
rs6590923	1.00[ASN][1000 genomes]
rs7101850	1.00[ASN][1000 genomes]
rs7117680	1.00[ASN][1000 genomes]
rs7925336	0.82[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7941166	1.00[ASN][1000 genomes]
rs7950837	0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs894256	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs894257	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs947993	1.00[ASN][1000 genomes]
rs947994	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1052159	chr11:101439655-101853293	Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1051457	chr11:101446705-101837650	Weak transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv530645	chr11:101451416-101778666	Bivalent/Poised TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv898332	chr11:101562004-101732566	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv832249	chr11:101571819-101749073	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv832250	chr11:101617934-101804020	Active TSS Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv430425	chr11:101626575-101741691	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr11:101723200-101723600	Active TSS	ES-WA7 Cell Line	embryonic stem cell

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