Variant report

Variant	rs7174447
Chromosome Location	chr15:53327727-53327728
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs12594246	0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1392858	0.85[ASN][1000 genomes]
rs1508045	0.83[ASN][1000 genomes]
rs17659077	0.87[ASN][1000 genomes]
rs17659107	0.85[ASN][1000 genomes]
rs2047667	0.89[ASN][1000 genomes]
rs2047668	0.89[ASN][1000 genomes]
rs2414224	0.91[ASN][1000 genomes]
rs2414227	0.84[ASN][1000 genomes]
rs4142454	0.87[ASN][1000 genomes]
rs73402033	0.88[ASN][1000 genomes]
rs73402040	0.87[ASN][1000 genomes]
rs73402043	0.86[ASN][1000 genomes]
rs73402051	0.86[ASN][1000 genomes]
rs73402072	0.83[ASN][1000 genomes]
rs8027120	0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8027138	0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8042629	0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs958059	0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv833007	chr15:53264564-53453525	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv904221	chr15:53279378-53434365	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	esv3343986	chr15:53284440-53571936	Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv569429	chr15:53301023-53329302	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv904222	chr15:53316487-53384700	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv1037630	chr15:53324645-53708925	Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
7	esv994129	chr15:53325369-53328207	Enhancers Flanking Active TSS	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:53326800-53327800	Enhancers	Liver	Liver
2	chr15:53327400-53328400	Enhancers	HepG2	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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