Variant report

Variant	rs72943227
Chromosome Location	chr3:100183078-100183079
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs72943223	1.00[EUR][1000 genomes]
rs72943225	0.98[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs72943232	0.81[AFR][1000 genomes]
rs72943233	0.81[AFR][1000 genomes]
rs72943234	1.00[EUR][1000 genomes]
rs73860607	1.00[EUR][1000 genomes]
rs73860651	1.00[EUR][1000 genomes]
rs73862460	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	nsv877218	chr3:100176360-100267619	Active TSS Weak transcription Enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 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	chr3:100172200-100185200	Weak transcription	Aorta	Aorta
2	chr3:100182000-100183200	Enhancers	NHEK	skin
3	chr3:100182200-100184800	Weak transcription	Liver	Liver
4	chr3:100183000-100184400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr3:100183000-100185000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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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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