Variant report

Variant	rs28473594
Chromosome Location	chr4:21511075-21511076
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10027808	0.82[AFR][1000 genomes]
rs1460479	0.89[AFR][1000 genomes]
rs1460480	0.95[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs1460481	0.98[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs16871265	0.82[AFR][1000 genomes]
rs16871286	0.88[AFR][1000 genomes]
rs16871288	0.99[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs16871289	0.99[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs16871290	0.99[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs16871292	0.99[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs28483282	0.98[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs28536057	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs28582299	0.97[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs28600372	0.97[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs28601719	0.97[AFR][1000 genomes]
rs28634569	0.96[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs28708392	0.99[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs6823425	0.82[AFR][1000 genomes]
rs6849960	0.81[AFR][1000 genomes]
rs6850575	0.82[AFR][1000 genomes]
rs73107977	0.99[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs9995812	0.98[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1013365	chr4:20834054-21609078	Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
2	nsv829879	chr4:21418568-21611002	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	2 gene(s)	inside rSNPs	diseases
3	nsv998481	chr4:21421945-21608805	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	2 gene(s)	inside rSNPs	diseases
4	nsv829880	chr4:21492426-21693816	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv878750	chr4:21492445-21520250	Enhancers Strong transcription Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:21497000-21514200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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