Variant report

Variant	rs9563181
Chromosome Location	chr13:54380670-54380671
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs1336925	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs17088940	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17088978	0.82[EUR][1000 genomes]
rs1870302	0.82[EUR][1000 genomes]
rs1932868	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2785824	0.84[EUR][1000 genomes]
rs2785825	0.83[EUR][1000 genomes]
rs2785827	0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2785828	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2785829	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2806723	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2806726	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2806728	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2806730	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7323659	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7327272	0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7327291	0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7328571	0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7989716	0.82[EUR][1000 genomes]
rs9316662	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs949944	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9568889	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9568921	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9568922	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9568925	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9568947	0.84[EUR][1000 genomes]
rs9634689	0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1044137	chr13:54124103-54521120	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv541777	chr13:54124103-54521120	Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	esv34743	chr13:54313729-54424593	Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	esv2757532	chr13:54333209-54421334	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	esv2759937	chr13:54333209-54421334	Enhancers Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv427931	chr13:54352943-54543848	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv826646	chr13:54355102-54423461	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv900092	chr13:54362624-54419426	Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr13:54380600-54381600	Enhancers	Fetal Heart	heart

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