Variant report

Variant	rs17136383
Chromosome Location	chr5:113544575-113544576
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:15)

rs_ID	r²[population]
rs12110041	0.97[AFR][1000 genomes]
rs12110045	0.97[AFR][1000 genomes]
rs12110221	0.81[AFR][1000 genomes]
rs12110227	0.81[AFR][1000 genomes]
rs17136330	0.81[AFR][1000 genomes]
rs17136332	0.81[AFR][1000 genomes]
rs17136340	0.81[AFR][1000 genomes]
rs17136361	0.97[AFR][1000 genomes]
rs17136382	1.00[AFR][1000 genomes]
rs28687690	1.00[AFR][1000 genomes]
rs4076578	0.81[AFR][1000 genomes]
rs4624786	1.00[AFR][1000 genomes]
rs6884723	0.97[AFR][1000 genomes]
rs7703150	0.97[AFR][1000 genomes]
rs7719362	0.97[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv882726	chr5:113404933-113555626	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv599432	chr5:113486177-113561766	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv981026	chr5:113539925-113544652	Enhancers Flanking Active TSS	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:113543600-113544600	Flanking Active TSS	Fetal Heart	heart

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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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