Variant report

Variant	rs28383792
Chromosome Location	chr9:21412074-21412075
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 69 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:63)

rs_ID	r²[population]
rs10114286	1.00[EUR][1000 genomes]
rs10121687	0.97[EUR][1000 genomes]
rs10125532	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11999696	0.81[EUR][1000 genomes]
rs12000461	1.00[AMR][1000 genomes]
rs12002231	1.00[AMR][1000 genomes]
rs12340196	0.97[EUR][1000 genomes]
rs1330321	1.00[EUR][1000 genomes]
rs28383780	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs28383791	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35000944	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs35353365	1.00[AMR][1000 genomes]
rs41270127	1.00[AMR][1000 genomes]
rs41270129	0.85[AMR][1000 genomes]
rs41270131	1.00[AMR][1000 genomes]
rs41270133	1.00[AMR][1000 genomes]
rs41270135	0.85[AMR][1000 genomes]
rs6475532	1.00[AMR][1000 genomes]
rs7037805	1.00[AMR][1000 genomes]
rs72691656	1.00[AMR][1000 genomes]
rs72691682	1.00[AMR][1000 genomes]
rs72691685	1.00[AMR][1000 genomes]
rs72691699	1.00[AMR][1000 genomes]
rs72691700	1.00[AMR][1000 genomes]
rs72691701	1.00[AMR][1000 genomes]
rs72691933	1.00[AMR][1000 genomes]
rs72691934	1.00[AMR][1000 genomes]
rs72691936	1.00[AMR][1000 genomes]
rs72691937	1.00[AMR][1000 genomes]
rs72691939	0.85[AMR][1000 genomes]
rs72691942	1.00[AMR][1000 genomes]
rs72691948	1.00[AMR][1000 genomes]
rs72693703	1.00[AMR][1000 genomes]
rs72693705	1.00[AMR][1000 genomes]
rs72695780	1.00[AMR][1000 genomes]
rs72695784	1.00[AMR][1000 genomes]
rs72695785	1.00[AMR][1000 genomes]
rs72695788	1.00[AMR][1000 genomes]
rs72695798	1.00[AMR][1000 genomes]
rs72695801	0.85[AMR][1000 genomes]
rs72697305	1.00[AMR][1000 genomes]
rs72697307	1.00[AMR][1000 genomes]
rs72697312	1.00[AMR][1000 genomes]
rs72697313	1.00[AMR][1000 genomes]
rs72697314	1.00[AMR][1000 genomes]
rs72697315	1.00[AMR][1000 genomes]
rs72697317	1.00[AMR][1000 genomes]
rs72697321	1.00[AMR][1000 genomes]
rs72697322	1.00[AMR][1000 genomes]
rs72697326	1.00[AMR][1000 genomes]
rs72697327	1.00[AMR][1000 genomes]
rs72699198	1.00[AMR][1000 genomes]
rs72701303	1.00[AMR][1000 genomes]
rs72701314	1.00[AMR][1000 genomes]
rs72701321	0.81[EUR][1000 genomes]
rs72701344	0.97[EUR][1000 genomes]
rs72701345	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs72701348	0.92[EUR][1000 genomes]
rs72701355	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72701357	1.00[EUR][1000 genomes]
rs72701366	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs72701368	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7862030	0.85[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv892724	chr9:20690244-21517302	Genic enhancers Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	153 gene(s)	inside rSNPs	diseases
2	esv2752289	chr9:21361957-21499624	Weak transcription Active TSS Enhancers Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
3	nsv892738	chr9:21371264-21413085	Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv466297	chr9:21391698-21507589	Enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
5	nsv613758	chr9:21391698-21507589	Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
6	nsv892739	chr9:21407250-21470520	Weak transcription Bivalent Enhancer ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 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	chr9:21412000-21412200	Flanking Active TSS	Primary B cells from cord blood	blood
2	chr9:21412000-21412400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr9:21412000-21412600	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr9:21412000-21412800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr9:21412000-21412800	Enhancers	Primary B cells from peripheral blood	blood
6	chr9:21412000-21413000	Enhancers	Brain Hippocampus Middle	brain
7	chr9:21412000-21413000	Enhancers	GM12878-XiMat	blood
8	chr9:21412000-21414000	Enhancers	Primary hematopoietic stem cells short term culture	blood

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