Variant report

Variant	rs73376581
Chromosome Location	chr7:79721011-79721012
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs59148543	0.89[AFR][1000 genomes]
rs6946197	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6949382	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6966043	0.87[AFR][1000 genomes]
rs73374551	0.83[AFR][1000 genomes]
rs73374586	0.84[AFR][1000 genomes]
rs73374587	0.81[AFR][1000 genomes]
rs73376514	0.87[AFR][1000 genomes]
rs73376517	0.84[AFR][1000 genomes]
rs73376520	0.84[AFR][1000 genomes]
rs73376537	0.86[AFR][1000 genomes]
rs73376566	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73376576	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73376578	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 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	nsv607678	chr7:79665817-79726578	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv1027494	chr7:79693976-79760332	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:79719800-79722000	Weak transcription	Fetal Lung	lung
2	chr7:79720800-79721400	Enhancers	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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