Variant report

Variant	rs3789134
Chromosome Location	chr2:111680155-111680156
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 143 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:133)

rs_ID	r²[population]
rs10164695	0.84[ASN][1000 genomes]
rs10165663	0.84[ASN][1000 genomes]
rs10168046	0.94[AFR][1000 genomes];0.85[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs10169926	0.84[ASN][1000 genomes]
rs10171765	0.80[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs10175204	0.84[ASN][1000 genomes]
rs10177582	0.84[ASN][1000 genomes]
rs10180551	0.90[ASN][1000 genomes]
rs10181923	0.84[ASN][1000 genomes]
rs10182055	0.84[ASN][1000 genomes]
rs10184452	0.84[ASN][1000 genomes]
rs10185326	0.84[ASN][1000 genomes]
rs10186144	0.84[ASN][1000 genomes]
rs10186627	0.81[ASN][1000 genomes]
rs10186753	0.84[ASN][1000 genomes]
rs10188079	0.80[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs10188169	0.89[ASN][1000 genomes]
rs10189620	0.84[ASN][1000 genomes]
rs10193050	0.90[ASN][1000 genomes]
rs10196268	0.89[ASN][1000 genomes]
rs10197135	0.84[ASN][1000 genomes]
rs10197140	0.90[ASN][1000 genomes]
rs10197548	0.84[ASN][1000 genomes]
rs10204997	0.84[ASN][1000 genomes]
rs10208020	0.84[ASN][1000 genomes]
rs11123211	0.89[ASN][1000 genomes]
rs11123221	0.84[ASN][1000 genomes]
rs11123227	0.80[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs11123229	0.84[ASN][1000 genomes]
rs11892748	0.90[ASN][1000 genomes]
rs11898005	0.88[ASN][1000 genomes]
rs12104528	0.84[ASN][1000 genomes]
rs12151613	0.90[ASN][1000 genomes]
rs12328918	0.84[ASN][1000 genomes]
rs12329097	0.89[ASN][1000 genomes]
rs12329103	0.89[ASN][1000 genomes]
rs12329216	0.89[ASN][1000 genomes]
rs12329344	0.89[ASN][1000 genomes]
rs12465068	0.89[ASN][1000 genomes]
rs12468564	0.90[ASN][1000 genomes]
rs12470827	0.84[ASN][1000 genomes]
rs12470872	0.84[ASN][1000 genomes]
rs12471566	0.89[ASN][1000 genomes]
rs12474757	0.89[ASN][1000 genomes]
rs12476335	0.89[ASN][1000 genomes]
rs12476386	0.84[ASN][1000 genomes]
rs12477660	0.89[ASN][1000 genomes]
rs13384044	0.84[ASN][1000 genomes]
rs13397744	0.84[ASN][1000 genomes]
rs13413838	0.86[AFR][1000 genomes]
rs13416355	0.89[ASN][1000 genomes]
rs13424637	0.84[ASN][1000 genomes]
rs13426283	0.89[ASN][1000 genomes]
rs13427098	0.89[ASN][1000 genomes]
rs13429695	0.84[ASN][1000 genomes]
rs13429892	0.84[ASN][1000 genomes]
rs1513825	0.83[ASN][1000 genomes]
rs1513826	0.86[ASN][1000 genomes]
rs1533296	0.80[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs17465162	0.90[ASN][1000 genomes]
rs17465210	0.90[ASN][1000 genomes]
rs17466548	0.90[ASN][1000 genomes]
rs17466576	0.86[ASN][1000 genomes]
rs17525147	0.88[ASN][1000 genomes]
rs17545048	0.81[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs17545166	0.90[ASN][1000 genomes]
rs17545286	0.90[ASN][1000 genomes]
rs1810229	0.88[ASN][1000 genomes]
rs1872062	0.84[ASN][1000 genomes]
rs2200211	0.89[ASN][1000 genomes]
rs2220092	0.89[ASN][1000 genomes]
rs2341897	0.89[ASN][1000 genomes]
rs28448691	0.84[ASN][1000 genomes]
rs28769005	0.80[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs28792074	0.89[ASN][1000 genomes]
rs2880192	0.96[AFR][1000 genomes];0.86[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs28806919	0.89[ASN][1000 genomes]
rs28811027	0.89[ASN][1000 genomes]
rs28855178	0.89[ASN][1000 genomes]
rs28855668	0.87[ASN][1000 genomes]
rs3761710	0.90[AFR][1000 genomes];0.84[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs3789130	0.86[AFR][1000 genomes];0.85[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs3789131	0.96[AFR][1000 genomes];0.85[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs4332932	0.90[ASN][1000 genomes]
rs4848344	0.84[AFR][1000 genomes]
rs4849120	0.90[ASN][1000 genomes]
rs4849162	0.84[ASN][1000 genomes]
rs4849164	0.83[ASN][1000 genomes]
rs4849165	0.84[ASN][1000 genomes]
rs4849170	0.83[ASN][1000 genomes]
rs4849201	0.90[ASN][1000 genomes]
rs4849203	0.81[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs57196449	0.88[ASN][1000 genomes]
rs62159471	0.90[ASN][1000 genomes]
rs62159472	0.84[ASN][1000 genomes]
rs62159473	0.84[ASN][1000 genomes]
rs62159474	0.84[ASN][1000 genomes]
rs62159500	0.89[ASN][1000 genomes]
rs62159501	0.89[ASN][1000 genomes]
rs62159502	0.89[ASN][1000 genomes]
rs62159503	0.89[ASN][1000 genomes]
rs62159553	0.90[ASN][1000 genomes]
rs62159554	0.86[ASN][1000 genomes]
rs62159555	0.86[ASN][1000 genomes]
rs62159556	0.81[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs6542188	0.84[ASN][1000 genomes]
rs6542189	0.84[ASN][1000 genomes]
rs6542190	0.84[ASN][1000 genomes]
rs6714299	0.90[ASN][1000 genomes]
rs6720034	0.86[ASN][1000 genomes]
rs6720503	0.90[ASN][1000 genomes]
rs6737631	0.89[ASN][1000 genomes]
rs6751930	0.89[ASN][1000 genomes]
rs6758344	0.89[ASN][1000 genomes]
rs72832894	0.89[ASN][1000 genomes]
rs7355443	0.84[ASN][1000 genomes]
rs7355554	0.84[ASN][1000 genomes]
rs750225	0.89[ASN][1000 genomes]
rs7563488	0.80[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs7569806	0.84[ASN][1000 genomes]
rs7609002	0.90[ASN][1000 genomes]
rs880506	0.80[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs880507	0.83[ASN][1000 genomes]
rs900556	0.90[ASN][1000 genomes]
rs900557	0.90[ASN][1000 genomes]
rs9308689	0.82[ASN][1000 genomes]
rs9308690	0.84[ASN][1000 genomes]
rs9308691	0.80[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs9308692	0.84[ASN][1000 genomes]
rs932076	0.84[ASN][1000 genomes]
rs932077	0.87[ASN][1000 genomes]
rs932078	0.89[ASN][1000 genomes]
rs999641	0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv874838	chr2:111376870-112046226	Weak transcription Strong transcription ZNF genes & repeats Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
2	nsv874839	chr2:111400934-111868010	Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv997829	chr2:111486961-111780537	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv834330	chr2:111593290-111789447	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv874840	chr2:111605245-111695479	Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv1004949	chr2:111607532-111780719	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv1002568	chr2:111607532-111781442	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv1005665	chr2:111610107-111762039	Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
9	nsv535892	chr2:111610107-111762039	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
10	nsv874841	chr2:111616304-111685789	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	Chromatin interactive region	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	chr2:111663000-111683800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr2:111679600-111681200	Enhancers	Adipose Nuclei	Adipose

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