Variant report

Variant	rs72934431
Chromosome Location	chr1:69990885-69990886
allele	C/T
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]
rs34176344	1.00[AMR][1000 genomes]
rs57703717	1.00[AMR][1000 genomes]
rs58099669	1.00[AMR][1000 genomes]
rs58877660	1.00[AMR][1000 genomes]
rs59878053	1.00[AMR][1000 genomes]
rs60213737	1.00[AMR][1000 genomes]
rs72932399	1.00[AFR][1000 genomes]
rs72934430	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72934438	1.00[AMR][1000 genomes]
rs72934441	1.00[AMR][1000 genomes]
rs72934459	1.00[AMR][1000 genomes]
rs72934498	1.00[AMR][1000 genomes]
rs72936507	1.00[AMR][1000 genomes]
rs72936520	1.00[AMR][1000 genomes]
rs72936533	1.00[AMR][1000 genomes]
rs72936595	1.00[AMR][1000 genomes]
rs72938926	1.00[AMR][1000 genomes]
rs72938944	1.00[AMR][1000 genomes]
rs72938946	1.00[AMR][1000 genomes]
rs72938951	1.00[AMR][1000 genomes]
rs72938953	1.00[AMR][1000 genomes]
rs72938959	1.00[AMR][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	nsv949691	chr1:69749722-70302201	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	esv3384194	chr1:69885024-70275430	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:69989000-69993800	Weak transcription	K562	blood
2	chr1:69990000-69993800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr1:69990000-69994200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr1:69990200-69994200	Weak transcription	HMEC	breast
5	chr1:69990200-69994200	Weak transcription	NHEK	skin
6	chr1:69990200-69994400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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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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