Variant report

Variant	rs57630850
Chromosome Location	chr5:8629066-8629067
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 59 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs10040042	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10040826	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10060970	0.90[EUR][1000 genomes]
rs10062575	0.93[EUR][1000 genomes]
rs10064896	0.93[EUR][1000 genomes]
rs10066543	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10071702	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10214050	0.93[EUR][1000 genomes]
rs12517710	0.84[EUR][1000 genomes]
rs12519783	0.84[EUR][1000 genomes]
rs12520885	0.84[EUR][1000 genomes]
rs13355566	0.88[EUR][1000 genomes]
rs13357083	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs13361593	0.88[EUR][1000 genomes]
rs1392958	0.88[EUR][1000 genomes]
rs1501346	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2388359	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2388360	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2388361	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2388362	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2388363	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2388364	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4404653	0.88[EUR][1000 genomes]
rs60499871	0.81[EUR][1000 genomes]
rs60571534	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs62355864	0.90[EUR][1000 genomes]
rs62357917	0.89[EUR][1000 genomes]
rs6859923	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6859933	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs722201	0.93[EUR][1000 genomes]
rs722202	0.93[EUR][1000 genomes]
rs722203	0.93[EUR][1000 genomes]
rs73738745	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs73738746	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7703856	0.84[EUR][1000 genomes]
rs7704554	0.81[EUR][1000 genomes]
rs7704712	0.84[EUR][1000 genomes]
rs7707778	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7708123	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7710782	0.83[EUR][1000 genomes]
rs7715870	0.83[AMR][1000 genomes]
rs7726627	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7728052	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7732493	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7732609	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7737474	0.93[EUR][1000 genomes]
rs9313248	0.93[EUR][1000 genomes]
rs9313250	0.93[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1033505	chr5:8258074-8657627	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases
2	nsv537634	chr5:8258074-8657627	ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases
3	nsv1026496	chr5:8275119-8681693	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	21 gene(s)	inside rSNPs	diseases
4	nsv537635	chr5:8275119-8681693	ZNF genes & repeats Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	21 gene(s)	inside rSNPs	diseases
5	nsv880933	chr5:8467174-8688962	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
6	nsv461929	chr5:8467900-8664747	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
7	nsv597028	chr5:8467900-8664747	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
8	nsv470987	chr5:8467900-8680327	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
9	nsv1032346	chr5:8522331-8747061	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	nsv537636	chr5:8522331-8747061	Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
11	nsv1033498	chr5:8554438-8702228	Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr5:8628600-8629200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr5:8628800-8629200	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr5:8628800-8629200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr5:8629000-8629200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr5:8629000-8629200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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