Variant report

Variant	rs7708592
Chromosome Location	chr5:151574040-151574041
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs56023602	1.00[AMR][1000 genomes]
rs58015776	1.00[AMR][1000 genomes]
rs58393037	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60253952	1.00[AMR][1000 genomes]
rs6881089	1.00[AMR][1000 genomes]
rs6883512	1.00[AMR][1000 genomes]
rs73796393	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73798027	1.00[AMR][1000 genomes]
rs73798033	1.00[AMR][1000 genomes]
rs73798043	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73798050	0.89[AFR][1000 genomes]
rs73798056	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73798057	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73798922	1.00[AMR][1000 genomes]
rs7718285	0.89[AFR][1000 genomes];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	esv2760935	chr5:151463117-151586051	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv883040	chr5:151471642-151596273	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1023828	chr5:151522149-151956217	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv5073	chr5:151551846-151597040	Enhancers Weak transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:151565600-151577800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr5:151573200-151574200	Weak transcription	Stomach Mucosa	stomach
3	chr5:151573400-151581600	Weak transcription	Pancreatic Islets	Pancreatic Islet

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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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