Variant report

Variant	rs59502095
Chromosome Location	chr18:13333558-13333559
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs58025644	1.00[AMR][1000 genomes]
rs59949510	1.00[AMR][1000 genomes]
rs60108757	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60389696	1.00[AMR][1000 genomes]
rs60756488	1.00[AMR][1000 genomes]
rs61460772	0.96[AFR][1000 genomes];1.00[AMR][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	nsv531246	chr18:13298774-14082028	Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 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	chr18:13320400-13338200	Weak transcription	Small Intestine	intestine
2	chr18:13321200-13336000	Weak transcription	Left Ventricle	heart
3	chr18:13323400-13335800	Weak transcription	Aorta	Aorta
4	chr18:13332000-13337600	Weak transcription	Thymus	Thymus
5	chr18:13332600-13336000	Weak transcription	Fetal Thymus	thymus

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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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