Variant report

Variant	rs73208183
Chromosome Location	chr7:116466634-116466635
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs56011846	1.00[ASN][1000 genomes]
rs56177042	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs62470806	1.00[ASN][1000 genomes]
rs6978286	1.00[ASN][1000 genomes]
rs73208144	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73208148	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73208158	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73208175	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73210117	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73210122	1.00[ASN][1000 genomes]
rs73210188	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73210190	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73210192	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73210195	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs7802141	1.00[ASN][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	nsv831107	chr7:116414734-116649466	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 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	chr7:116455600-116468400	Weak transcription	Liver	Liver

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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