Variant report

Variant	rs4133672
Chromosome Location	chr11:24894734-24894735
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 68 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:63)

rs_ID	r²[population]
rs10082639	0.85[EUR][1000 genomes]
rs10742053	0.84[EUR][1000 genomes]
rs10742054	0.81[EUR][1000 genomes]
rs10742055	0.82[EUR][1000 genomes]
rs10767265	0.92[EUR][1000 genomes]
rs10767267	0.91[EUR][1000 genomes]
rs10767268	0.92[EUR][1000 genomes]
rs10767271	0.82[EUR][1000 genomes]
rs10767272	0.84[EUR][1000 genomes]
rs10767275	0.83[EUR][1000 genomes]
rs10834521	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10834522	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10834527	0.89[CEU][hapmap]
rs10834533	0.84[EUR][1000 genomes]
rs10834535	0.84[EUR][1000 genomes]
rs10834537	0.84[EUR][1000 genomes]
rs10834538	0.84[EUR][1000 genomes]
rs10834540	0.81[EUR][1000 genomes]
rs10834541	0.81[EUR][1000 genomes]
rs10834542	0.81[EUR][1000 genomes]
rs10834543	0.83[EUR][1000 genomes]
rs11028244	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11028247	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11028248	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11028249	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11602437	0.84[EUR][1000 genomes]
rs12273099	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12785676	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1386231	0.92[EUR][1000 genomes]
rs1386232	0.92[EUR][1000 genomes]
rs1386234	1.00[CEU][hapmap];0.91[JPT][hapmap];0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1386235	0.85[CEU][hapmap]
rs2129356	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2129357	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2171256	0.91[EUR][1000 genomes]
rs2171257	0.89[EUR][1000 genomes]
rs2403988	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2403989	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2403990	0.88[EUR][1000 genomes]
rs2403991	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2896716	0.93[EUR][1000 genomes]
rs2896717	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs3598	0.88[EUR][1000 genomes]
rs3929310	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3958180	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs3992976	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4370935	0.93[EUR][1000 genomes]
rs4922701	0.89[EUR][1000 genomes]
rs61892071	0.92[EUR][1000 genomes]
rs7111460	0.84[EUR][1000 genomes]
rs7479243	0.85[EUR][1000 genomes]
rs7479940	0.84[EUR][1000 genomes]
rs749149	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs749150	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs749151	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs751170	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs766470	0.88[CEU][hapmap];0.84[EUR][1000 genomes]
rs7932867	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs901436	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9645612	0.92[EUR][1000 genomes]
rs972042	0.89[EUR][1000 genomes]
rs972043	0.88[EUR][1000 genomes]
rs972044	0.88[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1052730	chr11:24695821-25272497	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1053055	chr11:24700012-25293551	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	esv34111	chr11:24802669-25090774	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	esv34012	chr11:24831174-25090774	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv553827	chr11:24858636-25379281	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:24887000-24895400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr11:24893400-24894800	Enhancers	Pancreatic Islets	Pancreatic Islet
3	chr11:24893600-24895400	Enhancers	Adipose Nuclei	Adipose
4	chr11:24894400-24895400	Weak transcription	Fetal Lung	lung
5	chr11:24894600-24895400	Enhancers	Fetal Heart	heart

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