Variant report

Variant	rs28546731
Chromosome Location	chr4:172877311-172877312
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10021624	1.00[AMR][1000 genomes]
rs10021857	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10022562	1.00[AMR][1000 genomes]
rs10027525	1.00[AMR][1000 genomes]
rs10471194	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10471195	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10471196	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10471197	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13434610	1.00[AMR][1000 genomes]
rs13434620	1.00[AMR][1000 genomes]
rs13435186	1.00[AMR][1000 genomes]
rs13435577	1.00[AMR][1000 genomes]
rs28368507	1.00[AMR][1000 genomes]
rs28463325	1.00[AMR][1000 genomes]
rs28475852	1.00[AMR][1000 genomes]
rs28516370	1.00[AMR][1000 genomes]
rs28541484	1.00[AMR][1000 genomes]
rs28647375	1.00[AMR][1000 genomes]
rs28696751	1.00[AMR][1000 genomes]
rs28702744	1.00[AMR][1000 genomes]
rs28756913	1.00[AMR][1000 genomes]
rs58087716	1.00[AMR][1000 genomes]
rs61406189	1.00[AMR][1000 genomes]
rs6851131	1.00[AMR][1000 genomes]
rs9995741	1.00[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	nsv1022527	chr4:172547732-173236939	Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv537357	chr4:172547732-173236939	Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1024693	chr4:172609237-173236939	Active TSS Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv520744	chr4:172797761-172897603	Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv1029351	chr4:172809594-172893072	Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a
6	nsv498033	chr4:172830955-173121438	Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	3 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	chr4:172876400-172877800	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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