Variant report

Variant	rs6737139
Chromosome Location	chr2:189066854-189066855
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10931335	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs10931337	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs11890363	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs12463704	0.87[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs12467500	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs12619048	0.84[AMR][1000 genomes]
rs12994820	0.83[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs13002260	0.83[AMR][1000 genomes]
rs1371532	0.82[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs1371533	0.85[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs1439891	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs1439892	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs1439893	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs1439902	0.94[AMR][1000 genomes]
rs1439907	0.85[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs1898985	0.87[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs1975387	0.88[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs2119092	0.87[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs2119094	0.81[AMR][1000 genomes]
rs28781634	0.83[AMR][1000 genomes]
rs4312445	0.81[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs4527172	0.87[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs4666755	0.81[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs4666756	0.87[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs62181869	0.88[AMR][1000 genomes]
rs6434265	0.84[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs6706718	0.87[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs6707798	0.87[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs6710330	0.87[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs6725429	0.81[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs6726669	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs6727326	0.87[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs6737451	0.85[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs6737703	0.82[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs6740546	0.85[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs6742274	0.83[AMR][1000 genomes]
rs6746152	0.80[AFR][1000 genomes]
rs7567661	0.83[AMR][1000 genomes]
rs7573123	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs7597357	0.83[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs7601757	0.87[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs993209	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs997046	0.88[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1010394	chr2:188994398-189284092	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases
2	nsv875605	chr2:189017499-189080087	Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv998395	chr2:189018246-189284092	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:189061600-189067400	Weak transcription	Ovary	ovary
2	chr2:189061800-189069200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr2:189066000-189068600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr2:189066800-189069200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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