Variant report

Variant	rs9369759
Chromosome Location	chr6:13020686-13020687
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:13019900..13022140-chr6:13027831..13030315,2	K562	blood:

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10807388	0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11758659	0.90[EUR][1000 genomes]
rs12216401	0.94[ASN][1000 genomes]
rs1579135	0.89[ASN][1000 genomes]
rs1937771	0.91[ASN][1000 genomes]
rs34576660	0.83[EUR][1000 genomes]
rs4132046	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4236097	0.82[EUR][1000 genomes]
rs4292514	0.94[ASN][1000 genomes]
rs4349811	0.91[EUR][1000 genomes]
rs4357136	0.91[ASN][1000 genomes]
rs4367379	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4432976	0.94[ASN][1000 genomes]
rs4492189	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4580867	0.94[ASN][1000 genomes]
rs4624870	0.92[ASN][1000 genomes]
rs4715048	0.91[EUR][1000 genomes]
rs5002331	0.94[ASN][1000 genomes]
rs6924689	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7341250	0.90[EUR][1000 genomes]
rs7738606	0.94[ASN][1000 genomes]
rs7748124	0.80[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs9349456	0.94[ASN][1000 genomes]
rs9369760	0.90[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9369768	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9369779	0.89[ASN][1000 genomes]
rs9369815	0.91[ASN][1000 genomes]
rs9381636	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9395335	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9463363	0.91[EUR][1000 genomes]
rs9463364	0.90[EUR][1000 genomes]
rs9473198	0.91[EUR][1000 genomes]
rs9473437	0.91[ASN][1000 genomes]
rs9473486	0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3521000	chr6:12561306-13128519	Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	esv3521001	chr6:12561306-13128519	Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv817350	chr6:12922859-13137655	Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
4	nsv600992	chr6:12961922-13218549	Weak transcription Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:13015000-13026000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr6:13015000-13026400	Weak transcription	Primary hematopoietic stem cells	blood
3	chr6:13015200-13024400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr6:13015400-13024400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr6:13015600-13023400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr6:13015600-13027600	Weak transcription	Right Atrium	heart
7	chr6:13015800-13024600	Weak transcription	Brain Angular Gyrus	brain
8	chr6:13015800-13024600	Weak transcription	Brain Cingulate Gyrus	brain
9	chr6:13015800-13029000	Weak transcription	Pancreas	Pancrea
10	chr6:13016200-13021000	Weak transcription	Aorta	Aorta
11	chr6:13016200-13025800	Weak transcription	Fetal Brain Female	brain
12	chr6:13016200-13025800	Weak transcription	Stomach Smooth Muscle	stomach
13	chr6:13016400-13023600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr6:13016400-13023800	Weak transcription	Brain Anterior Caudate	brain
15	chr6:13018800-13020800	Enhancers	Fetal Heart	heart
16	chr6:13018800-13023800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
17	chr6:13020000-13021800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr6:13020200-13021200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
19	chr6:13020200-13021200	Enhancers	Right Ventricle	heart
20	chr6:13020600-13020800	Enhancers	Left Ventricle	heart

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