Variant report

Variant	rs73207117
Chromosome Location	chr8:9686850-9686851
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs11786541	1.00[ASN][1000 genomes]
rs13282752	1.00[ASN][1000 genomes]
rs17150816	1.00[ASN][1000 genomes]
rs60121567	1.00[ASN][1000 genomes]
rs66536005	1.00[ASN][1000 genomes]
rs73189109	1.00[ASN][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	nsv530864	chr8:9097498-9914548	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
2	esv16865	chr8:9642195-9712807	Enhancers Active TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 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	chr8:9684200-9689000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr8:9685200-9687800	Enhancers	HepG2	liver
3	chr8:9686600-9687000	Enhancers	Fetal Stomach	stomach
4	chr8:9686600-9687000	Enhancers	NHEK	skin
5	chr8:9686600-9687800	Weak transcription	A549	lung

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dbSNP/dbVar ID: rs12345 /nsv7879
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