Variant report

Variant	rs58160513
Chromosome Location	chr4:129514105-129514106
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:16)

rs_ID	r²[population]
rs17013484	0.93[EUR][1000 genomes]
rs17013486	0.93[EUR][1000 genomes]
rs57357435	0.93[EUR][1000 genomes]
rs57404895	0.88[ASN][1000 genomes]
rs57673046	0.94[ASN][1000 genomes]
rs58200674	0.93[EUR][1000 genomes]
rs59261281	0.93[EUR][1000 genomes]
rs60593095	0.93[EUR][1000 genomes]
rs60917665	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs60972557	0.93[EUR][1000 genomes]
rs72932244	0.81[EUR][1000 genomes]
rs72932252	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72932254	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72932256	0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs72932257	0.93[EUR][1000 genomes]
rs73846936	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869258	chr4:129191619-130138148	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	79 gene(s)	inside rSNPs	diseases
2	nsv1017672	chr4:129450450-129603977	Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:129505800-129520400	Weak transcription	Gastric	stomach
2	chr4:129510000-129514200	Enhancers	Fetal Heart	heart
3	chr4:129511800-129519800	Weak transcription	Right Ventricle	heart
4	chr4:129512200-129517200	Weak transcription	Stomach Mucosa	stomach
5	chr4:129512400-129518400	Weak transcription	Stomach Smooth Muscle	stomach
6	chr4:129512800-129520400	Weak transcription	Left Ventricle	heart
7	chr4:129513000-129517200	Weak transcription	A549	lung
8	chr4:129513800-129515600	Weak transcription	Pancreas	Pancrea

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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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