Variant report

Variant	rs73856574
Chromosome Location	chr3:98023988-98023989
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 70 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1603598	1.00[AMR][1000 genomes]
rs1846079	1.00[AMR][1000 genomes]
rs1846080	1.00[AMR][1000 genomes]
rs4582089	1.00[AMR][1000 genomes]
rs55696575	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55985096	1.00[AMR][1000 genomes]
rs57361363	1.00[AMR][1000 genomes]
rs58415495	1.00[AMR][1000 genomes]
rs59518469	1.00[AMR][1000 genomes]
rs60154921	1.00[AMR][1000 genomes]
rs60579668	1.00[AMR][1000 genomes]
rs60579974	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73854599	1.00[AMR][1000 genomes]
rs73854600	1.00[AMR][1000 genomes]
rs73854601	1.00[AMR][1000 genomes]
rs73854602	1.00[AMR][1000 genomes]
rs73854623	1.00[AMR][1000 genomes]
rs73854624	1.00[AMR][1000 genomes]
rs73854625	1.00[AMR][1000 genomes]
rs73854626	1.00[AMR][1000 genomes]
rs73854627	1.00[AMR][1000 genomes]
rs73854628	1.00[AMR][1000 genomes]
rs73856504	1.00[AMR][1000 genomes]
rs73856505	1.00[AMR][1000 genomes]
rs73856506	1.00[AMR][1000 genomes]
rs73856507	1.00[AMR][1000 genomes]
rs73856508	1.00[AMR][1000 genomes]
rs73856509	1.00[AMR][1000 genomes]
rs73856510	1.00[AMR][1000 genomes]
rs73856517	1.00[AMR][1000 genomes]
rs73856518	1.00[AMR][1000 genomes]
rs73856520	1.00[AMR][1000 genomes]
rs73856521	1.00[AMR][1000 genomes]
rs73856522	1.00[AMR][1000 genomes]
rs73856523	1.00[AMR][1000 genomes]
rs73856524	1.00[AMR][1000 genomes]
rs73856525	1.00[AMR][1000 genomes]
rs73856527	1.00[AMR][1000 genomes]
rs73856528	1.00[AMR][1000 genomes]
rs73856530	1.00[AMR][1000 genomes]
rs73856532	1.00[AMR][1000 genomes]
rs73856533	1.00[AMR][1000 genomes]
rs73856534	1.00[AMR][1000 genomes]
rs73856536	1.00[AMR][1000 genomes]
rs73856538	1.00[AMR][1000 genomes]
rs73856540	1.00[AMR][1000 genomes]
rs73856542	1.00[AMR][1000 genomes]
rs73856546	1.00[AMR][1000 genomes]
rs73856547	1.00[AMR][1000 genomes]
rs73856548	1.00[AMR][1000 genomes]
rs73856550	1.00[AMR][1000 genomes]
rs73856553	1.00[AMR][1000 genomes]
rs73856569	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73857409	1.00[AMR][1000 genomes]
rs73857410	1.00[AMR][1000 genomes]
rs73857411	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73857413	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73857414	1.00[AMR][1000 genomes]
rs73857415	1.00[AMR][1000 genomes]
rs7432818	1.00[AMR][1000 genomes]
rs7632428	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869347	chr3:97742604-98051633	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
2	nsv877209	chr3:97806616-98049409	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	nsv963576	chr3:97825434-98041343	Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
4	nsv1004820	chr3:97852875-98169488	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
5	nsv834773	chr3:97855362-98043888	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
6	nsv1000834	chr3:97859880-98095473	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
7	nsv877212	chr3:97931105-98033400	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
8	esv1842860	chr3:97934241-98075543	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
9	nsv1009918	chr3:97946030-98155450	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:98023800-98024000	Enhancers	ES-I3 Cell Line	embryonic stem cell

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