Variant report

Variant	rs57696204
Chromosome Location	chr2:53473459-53473460
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs1118769	0.96[EUR][1000 genomes]
rs17044370	1.00[AMR][1000 genomes]
rs17044373	1.00[AMR][1000 genomes]
rs58487531	0.96[EUR][1000 genomes]
rs58772874	0.81[EUR][1000 genomes]
rs59463716	1.00[AMR][1000 genomes]
rs59617749	1.00[AMR][1000 genomes]
rs60446757	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60701616	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6712763	0.85[AMR][1000 genomes]
rs73936015	1.00[AMR][1000 genomes]
rs73936016	1.00[AMR][1000 genomes]
rs73936017	1.00[AMR][1000 genomes]
rs73936025	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2751897	chr2:53358205-53475338	Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
2	nsv1002145	chr2:53387912-53832213	Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv535718	chr2:53387912-53832213	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv1013201	chr2:53473426-53553384	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	2 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	chr2:53471800-53480400	Weak transcription	Pancreas	Pancrea

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

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