Variant report

Variant	rs59920410
Chromosome Location	chr7:80024040-80024041
allele	A/C
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:7)

rs_ID	r²[population]
rs59820812	1.00[AMR][1000 genomes]
rs61501316	1.00[AMR][1000 genomes]
rs73384709	1.00[AMR][1000 genomes]
rs73384747	1.00[AMR][1000 genomes]
rs73384762	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73384771	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7789248	0.89[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	nsv429785	chr7:79589749-80177049	Bivalent/Poised TSS Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv831042	chr7:79984079-80122312	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 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	chr7:80017200-80029400	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr7:80021400-80024200	Weak transcription	Fetal Brain Female	brain
3	chr7:80022600-80025000	Weak transcription	Fetal Brain Male	brain
4	chr7:80023600-80024200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr7:80023600-80029600	Weak transcription	Liver	Liver

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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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