Variant report

Variant	rs2186607
Chromosome Location	chr11:101656397-101656398
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10501990	0.84[AMR][1000 genomes]
rs10791523	0.83[AMR][1000 genomes]
rs10791524	0.83[AMR][1000 genomes]
rs10895192	0.85[AMR][1000 genomes]
rs10895202	0.81[AMR][1000 genomes]
rs12577395	0.83[ASN][1000 genomes]
rs17097081	0.85[ASN][1000 genomes]
rs17097133	0.85[ASN][1000 genomes]
rs1939026	0.89[ASN][1000 genomes]
rs1939027	0.89[ASN][1000 genomes]
rs1939031	0.82[AMR][1000 genomes]
rs1939036	0.81[AMR][1000 genomes]
rs1939041	0.83[AMR][1000 genomes]
rs1939044	0.87[AMR][1000 genomes]
rs1939045	0.87[AMR][1000 genomes]
rs1939056	0.83[AMR][1000 genomes]
rs1939060	0.86[ASN][1000 genomes]
rs1939063	0.85[AMR][1000 genomes]
rs1939069	0.83[AMR][1000 genomes]
rs1939070	0.88[AMR][1000 genomes]
rs1939461	0.87[AMR][1000 genomes]
rs2000535	0.81[AMR][1000 genomes]
rs2155064	0.84[AMR][1000 genomes]
rs2155065	0.88[EUR][1000 genomes]
rs2155066	0.83[AMR][1000 genomes]
rs2186608	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2226573	0.89[ASN][1000 genomes]
rs2226574	0.89[ASN][1000 genomes]
rs3891473	0.83[ASN][1000 genomes]
rs4084123	0.86[AMR][1000 genomes]
rs4237604	0.81[AMR][1000 genomes]
rs4450143	0.89[ASN][1000 genomes]
rs4754020	0.84[AMR][1000 genomes]
rs4754021	0.83[AMR][1000 genomes]
rs4754799	0.87[AMR][1000 genomes]
rs4754802	0.84[AMR][1000 genomes]
rs4754805	0.81[AMR][1000 genomes]
rs56188046	0.85[ASN][1000 genomes]
rs59641563	0.89[ASN][1000 genomes]
rs60192666	0.83[ASN][1000 genomes]
rs61053262	0.89[ASN][1000 genomes]
rs6590920	0.87[AMR][1000 genomes]
rs6590923	0.82[AMR][1000 genomes]
rs7101850	0.83[AMR][1000 genomes]
rs7117680	0.83[AMR][1000 genomes]
rs731593	0.85[ASN][1000 genomes]
rs732087	0.86[ASN][1000 genomes]
rs744808	0.86[ASN][1000 genomes]
rs947993	0.88[AMR][1000 genomes]
rs947994	0.88[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv898330	chr11:101243644-101722031	Enhancers Bivalent/Poised TSS Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
2	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
3	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
4	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
5	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
6	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
7	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
8	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:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:101655200-101657200	Weak transcription	Psoas Muscle	Psoas
2	chr11:101656000-101656800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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