Variant report

Variant	rs58474198
Chromosome Location	chr5:36354498-36354499
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs10042470	1.00[EUR][1000 genomes]
rs10050988	1.00[EUR][1000 genomes]
rs10213853	1.00[EUR][1000 genomes]
rs13358189	1.00[EUR][1000 genomes]
rs13359855	1.00[EUR][1000 genomes]
rs28469511	1.00[EUR][1000 genomes]
rs28564846	1.00[EUR][1000 genomes]
rs6875408	1.00[EUR][1000 genomes]
rs73748605	1.00[EUR][1000 genomes]
rs7704701	1.00[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv881598	chr5:36248752-36382802	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:36344400-36362000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr5:36346800-36357200	Weak transcription	Fetal Lung	lung
3	chr5:36347000-36355200	Weak transcription	Hela-S3	cervix
4	chr5:36354200-36355000	Weak transcription	Esophagus	oesophagus
5	chr5:36354400-36354600	Enhancers	NHEK	skin

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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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