Variant report

Variant	rs56356828
Chromosome Location	chr3:54652743-54652744
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 27 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10510769	0.92[EUR][1000 genomes]
rs10510770	0.91[EUR][1000 genomes]
rs1130197	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs17054227	0.90[EUR][1000 genomes]
rs17815617	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2359857	0.87[EUR][1000 genomes]
rs2884808	0.86[EUR][1000 genomes]
rs4345041	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4386460	0.90[EUR][1000 genomes]
rs55772258	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs55779022	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs56008232	0.88[EUR][1000 genomes]
rs56091855	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs56209938	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs56260111	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs56976748	0.84[EUR][1000 genomes]
rs62255527	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs62255532	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs62255533	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs62255534	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs62255535	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs62255538	0.81[EUR][1000 genomes]
rs6803005	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs73068445	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1014595	chr3:53944473-54846754	Enhancers Bivalent Enhancer Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv428084	chr3:54404258-54742756	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv834700	chr3:54637374-54803896	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs56356828	ESRG	cis	Whole Blood	GTEx

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:54646800-54655200	Weak transcription	Brain Angular Gyrus	brain
2	chr3:54650400-54654600	Weak transcription	Fetal Muscle Trunk	muscle
3	chr3:54651000-54666400	Weak transcription	H9 Cell Line	embryonic stem cell

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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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