Variant report

Variant	rs72888080
Chromosome Location	chr4:98141412-98141413
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs72885916	1.00[AMR][1000 genomes]
rs72885924	1.00[AMR][1000 genomes]
rs72885931	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72885980	0.80[AFR][1000 genomes]
rs72885984	0.80[AFR][1000 genomes]
rs72885987	0.80[AFR][1000 genomes]
rs72885989	0.80[AFR][1000 genomes]
rs72885993	0.80[AFR][1000 genomes]
rs72886000	0.80[AFR][1000 genomes]
rs72888010	0.80[AFR][1000 genomes]
rs72888017	0.82[AFR][1000 genomes]
rs72888019	0.82[AFR][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	nsv879640	chr4:97711707-98697586	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 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	chr4:98141000-98142000	Weak transcription	Placenta Amnion	Placenta Amnion

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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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