Variant report

Variant	rs9568069
Chromosome Location	chr13:49209632-49209633
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs1009717	0.82[ASN][1000 genomes]
rs1009718	0.82[ASN][1000 genomes]
rs11840006	0.85[ASN][1000 genomes]
rs12867213	0.83[ASN][1000 genomes]
rs12874937	0.83[ASN][1000 genomes]
rs1323556	0.88[ASN][1000 genomes]
rs1575464	0.88[ASN][1000 genomes]
rs1575465	0.88[ASN][1000 genomes]
rs1575920	0.82[ASN][1000 genomes]
rs1854017	0.82[ASN][1000 genomes]
rs2406937	0.82[ASN][1000 genomes]
rs2406938	0.83[ASN][1000 genomes]
rs2406939	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2407093	0.82[AFR][1000 genomes]
rs2407246	0.88[ASN][1000 genomes]
rs2897623	0.88[ASN][1000 genomes]
rs3945837	0.87[ASN][1000 genomes]
rs4451857	0.82[ASN][1000 genomes]
rs4942769	0.90[ASN][1000 genomes]
rs6561469	0.82[ASN][1000 genomes]
rs7318887	0.80[ASN][1000 genomes]
rs7323160	0.88[ASN][1000 genomes]
rs7324562	0.81[ASN][1000 genomes]
rs7332030	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7336379	0.82[AFR][1000 genomes]
rs7990619	0.82[ASN][1000 genomes]
rs7990660	0.82[ASN][1000 genomes]
rs8000783	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs8001736	0.83[ASN][1000 genomes]
rs8002035	0.83[ASN][1000 genomes]
rs9535059	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9535060	0.83[ASN][1000 genomes]
rs9562833	0.82[ASN][1000 genomes]
rs9568056	0.82[ASN][1000 genomes]
rs9568058	0.82[ASN][1000 genomes]
rs9568059	1.00[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs9568061	0.81[ASN][1000 genomes]
rs9568062	0.82[ASN][1000 genomes]
rs9568064	0.83[ASN][1000 genomes]
rs9568065	0.83[ASN][1000 genomes]
rs9591187	0.83[ASN][1000 genomes]
rs9595937	0.90[AFR][1000 genomes]
rs9595943	0.83[ASN][1000 genomes]
rs9595944	0.83[ASN][1000 genomes]
rs9595945	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs964413	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[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	nsv1041275	chr13:49045566-49242357	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv541769	chr13:49045566-49242357	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Genic enhancers Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
3	nsv832604	chr13:49061081-49281807	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
4	nsv1049117	chr13:49089476-49928945	Enhancers Strong transcription Weak transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
5	nsv832605	chr13:49171305-49344970	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
6	esv3495983	chr13:49181790-49222165	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
7	esv3495984	chr13:49181790-49222165	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:49201600-49210200	Weak transcription	Fetal Kidney	kidney
2	chr13:49202200-49210400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr13:49205000-49210400	Weak transcription	Stomach Mucosa	stomach
4	chr13:49207600-49210800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr13:49208800-49210400	Weak transcription	Adipose Nuclei	Adipose
6	chr13:49208800-49210800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr13:49208800-49213200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr13:49209400-49210600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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