Variant report

Variant	rs72767434
Chromosome Location	chr5:57028952-57028953
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10447121	0.82[EUR][1000 genomes]
rs10940574	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12514617	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12514618	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12515493	0.82[EUR][1000 genomes]
rs12517867	0.82[EUR][1000 genomes]
rs12520466	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12522697	0.85[EUR][1000 genomes]
rs12523004	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1544621	0.82[EUR][1000 genomes]
rs17689645	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs17689832	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2160057	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2160058	0.82[EUR][1000 genomes]
rs2192367	0.85[EUR][1000 genomes]
rs2192368	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2898027	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs58610852	0.81[EUR][1000 genomes]
rs58632739	0.82[EUR][1000 genomes]
rs62358372	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs62358374	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs62358380	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62358381	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs62361169	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6450432	0.82[EUR][1000 genomes]
rs6450433	0.82[EUR][1000 genomes]
rs6450434	0.82[EUR][1000 genomes]
rs6450435	0.82[EUR][1000 genomes]
rs6870485	0.85[EUR][1000 genomes]
rs6891648	0.82[EUR][1000 genomes]
rs6894116	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs72767430	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs72767441	0.83[EUR][1000 genomes]
rs72767444	0.82[EUR][1000 genomes]
rs741181	0.83[EUR][1000 genomes]
rs7718447	0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv525330	chr5:56931673-57320343	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	esv2756302	chr5:56978143-57180143	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv830310	chr5:56989346-57176006	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	esv2763454	chr5:57006531-57161140	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr5:57021800-57029200	Weak transcription	Aorta	Aorta
2	chr5:57021800-57030400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr5:57028600-57030000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr5:57028600-57031200	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr5:57028800-57029000	Enhancers	Fetal Lung	lung

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