Variant report

Variant	rs9884794
Chromosome Location	chr4:47760334-47760335
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10003421	1.00[AMR][1000 genomes]
rs10007715	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10008612	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10017737	0.82[AFR][1000 genomes]
rs10018986	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10021423	1.00[AFR][1000 genomes]
rs10028438	0.80[AFR][1000 genomes]
rs10031604	0.81[AFR][1000 genomes]
rs28414198	0.83[AFR][1000 genomes]
rs28455705	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28474765	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28506797	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28574870	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28671484	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28736683	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28762675	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28817328	0.91[AFR][1000 genomes]
rs28841313	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs3924199	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs3924200	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4131787	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6822826	1.00[AMR][1000 genomes]
rs7675724	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7681031	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7697926	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9291315	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9291316	0.82[AFR][1000 genomes]
rs9884743	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9884844	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9942274	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9995873	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9996270	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9996567	0.81[AFR][1000 genomes]
rs9996629	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1008515	chr4:47488431-47906835	Weak transcription Strong transcription Flanking Bivalent TSS/Enh Enhancers Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	nsv948568	chr4:47488431-47907524	Enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv1004939	chr4:47488573-47901460	Bivalent Enhancer Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv537080	chr4:47488573-47901460	Weak transcription Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
5	nsv997471	chr4:47489412-47895223	Weak transcription Strong transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
6	nsv998892	chr4:47493552-47863354	Weak transcription Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
7	nsv537081	chr4:47493552-47863354	Strong transcription Weak transcription Enhancers Bivalent/Poised TSS Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
8	nsv1000337	chr4:47493907-47902019	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
9	nsv594118	chr4:47560386-47917730	Weak transcription Strong transcription Bivalent/Poised TSS ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	12 gene(s)	inside rSNPs	diseases
10	nsv829924	chr4:47670905-47866665	Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:47755400-47763200	Weak transcription	Muscle Satellite Cultured Cells	--
2	chr4:47759000-47761800	Weak transcription	Fetal Heart	heart

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