Variant report

Variant	rs58937051
Chromosome Location	chr7:14122475-14122476
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs17167840	1.00[AMR][1000 genomes]
rs57238832	1.00[AMR][1000 genomes]
rs57254960	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58997086	1.00[AMR][1000 genomes]
rs59565101	1.00[AMR][1000 genomes]
rs60121356	1.00[AMR][1000 genomes]
rs60787150	1.00[AMR][1000 genomes]
rs60917785	1.00[AMR][1000 genomes]
rs61100266	1.00[AMR][1000 genomes]
rs61474076	1.00[AMR][1000 genomes]
rs73268004	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73268020	1.00[AMR][1000 genomes]
rs73268021	1.00[AMR][1000 genomes]
rs73278802	1.00[AMR][1000 genomes]
rs73280538	1.00[AMR][1000 genomes]
rs73280580	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	nsv1019873	chr7:13707148-14133367	Bivalent Enhancer Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv949467	chr7:13938464-14279074	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv949033	chr7:14086106-14860323	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv1015312	chr7:14092753-14266917	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	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	chr7:14121200-14123000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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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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