Variant report

Variant	rs55913729
Chromosome Location	chr5:30196190-30196191
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs11948380	1.00[EUR][1000 genomes]
rs11953269	0.83[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs11958611	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs16899990	1.00[EUR][1000 genomes]
rs28870420	0.99[EUR][1000 genomes]
rs4282330	0.95[EUR][1000 genomes]
rs4337863	0.99[EUR][1000 genomes]
rs4343853	0.99[EUR][1000 genomes]
rs4386744	1.00[EUR][1000 genomes]
rs4605801	0.96[EUR][1000 genomes]
rs57503003	0.95[EUR][1000 genomes]
rs58624784	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs59615654	0.95[EUR][1000 genomes]
rs60373268	0.80[EUR][1000 genomes]
rs6872827	0.97[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73084983	0.99[EUR][1000 genomes]
rs73754648	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs73754668	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73755029	0.86[AMR][1000 genomes]
rs7733219	1.00[EUR][1000 genomes]
rs7733353	0.99[EUR][1000 genomes]
rs7735950	0.99[EUR][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	nsv881635	chr5:30122190-30371238	Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv915858	chr5:30176470-31018294	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS	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	chr5:30195800-30198000	Weak transcription	Pancreatic Islets	Pancreatic Islet

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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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