Variant report

Variant	rs73303384
Chromosome Location	chr5:124786620-124786621
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 63 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:61)

rs_ID	r²[population]
rs1554281	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55717300	1.00[AMR][1000 genomes]
rs56707415	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56821497	1.00[AMR][1000 genomes]
rs56835569	1.00[AMR][1000 genomes]
rs56988571	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57118683	1.00[AMR][1000 genomes]
rs57123863	1.00[AMR][1000 genomes]
rs57697012	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58308815	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58338793	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58631543	1.00[AMR][1000 genomes]
rs58917396	1.00[AMR][1000 genomes]
rs59000628	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59380738	1.00[AMR][1000 genomes]
rs59958060	1.00[EUR][1000 genomes]
rs60202964	1.00[EUR][1000 genomes]
rs60214755	1.00[AMR][1000 genomes]
rs61304237	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61472360	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6595615	1.00[AMR][1000 genomes]
rs6866932	0.84[AFR][1000 genomes]
rs6866980	0.83[AFR][1000 genomes]
rs6870489	1.00[AMR][1000 genomes]
rs6875057	0.83[AFR][1000 genomes]
rs6875229	0.83[AFR][1000 genomes]
rs6878929	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6883449	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6883628	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6884059	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6884354	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6890153	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6894842	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73303305	0.83[AFR][1000 genomes]
rs73303332	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73303334	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73303374	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73303399	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73303400	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73305305	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73305308	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73305320	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73305337	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73305339	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73305342	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73305345	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73305365	1.00[EUR][1000 genomes]
rs73305368	1.00[EUR][1000 genomes]
rs73305401	1.00[EUR][1000 genomes]
rs73307316	1.00[EUR][1000 genomes]
rs73312635	1.00[EUR][1000 genomes]
rs73321471	0.84[AFR][1000 genomes]
rs73321473	0.83[AFR][1000 genomes]
rs7702589	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7711951	1.00[AMR][1000 genomes]
rs7725952	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7729702	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7729817	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7730376	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7730445	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7732317	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1030992	chr5:124708549-125391503	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv537892	chr5:124708549-125391503	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:124785600-124789000	Enhancers	Fetal Brain Male	brain
2	chr5:124785800-124786800	Enhancers	Fetal Brain Female	brain
3	chr5:124786400-124787000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr5:124786400-124787000	Enhancers	Fetal Stomach	stomach
5	chr5:124786400-124787000	Enhancers	NHLF	lung
6	chr5:124786400-124787200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr5:124786400-124787200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr5:124786600-124786800	Enhancers	Fetal Lung	lung

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