Variant report

Variant	rs10111769
Chromosome Location	chr8:20958756-20958757
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10112502	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10503698	0.82[ASN][1000 genomes]
rs11784441	0.81[ASN][1000 genomes]
rs11996651	0.81[ASN][1000 genomes]
rs12674821	0.81[ASN][1000 genomes]
rs12675109	0.80[ASN][1000 genomes]
rs12677314	0.82[ASN][1000 genomes]
rs12678981	0.83[ASN][1000 genomes]
rs12679819	0.81[ASN][1000 genomes]
rs12679855	0.81[ASN][1000 genomes]
rs12680270	0.81[ASN][1000 genomes]
rs12680287	0.81[ASN][1000 genomes]
rs13250583	0.81[ASN][1000 genomes]
rs13258422	0.81[ASN][1000 genomes]
rs13276143	0.88[ASN][1000 genomes]
rs13282584	0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1563919	0.81[ASN][1000 genomes]
rs1563920	0.81[ASN][1000 genomes]
rs1563921	0.81[ASN][1000 genomes]
rs1841510	0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs34133224	0.81[ASN][1000 genomes]
rs34402513	0.81[ASN][1000 genomes]
rs34437032	0.80[ASN][1000 genomes]
rs35089394	0.80[ASN][1000 genomes]
rs35393501	0.97[ASN][1000 genomes]
rs35508548	0.85[ASN][1000 genomes]
rs35555613	0.81[ASN][1000 genomes]
rs35842344	0.86[ASN][1000 genomes]
rs35923081	0.93[ASN][1000 genomes]
rs3903353	0.87[ASN][1000 genomes]
rs4739209	0.81[ASN][1000 genomes]
rs57399105	0.83[ASN][1000 genomes]
rs59048764	0.88[ASN][1000 genomes]
rs6985275	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7015657	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7839300	0.81[ASN][1000 genomes]
rs898648	0.96[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	nsv1032450	chr8:20514995-21033577	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv539524	chr8:20514995-21033577	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	nsv1034265	chr8:20742935-21152545	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
4	nsv539528	chr8:20742935-21152545	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
5	nsv831260	chr8:20907266-21097125	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv469878	chr8:20955260-21128307	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv482339	chr8:20955260-21128307	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:20956400-20959000	Enhancers	Skeletal Muscle Male	skeletal muscle
2	chr8:20956400-20959600	Enhancers	Fetal Brain Male	brain
3	chr8:20956600-20958800	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr8:20956600-20959400	Enhancers	Colon Smooth Muscle	Colon
5	chr8:20956600-20959600	Enhancers	Brain Germinal Matrix	brain
6	chr8:20956800-20958800	Enhancers	Left Ventricle	heart
7	chr8:20956800-20959600	Enhancers	Fetal Heart	heart
8	chr8:20957000-20959200	Enhancers	Rectal Smooth Muscle	rectum
9	chr8:20957200-20958800	Enhancers	Duodenum Smooth Muscle	Duodenum
10	chr8:20957600-20959000	Enhancers	Aorta	Aorta
11	chr8:20957600-20959000	Enhancers	Stomach Smooth Muscle	stomach
12	chr8:20958000-20959800	Enhancers	Fetal Brain Female	brain
13	chr8:20958200-20958800	Enhancers	Adipose Nuclei	Adipose
14	chr8:20958200-20958800	Enhancers	Fetal Muscle Trunk	muscle
15	chr8:20958400-20958800	Enhancers	Brain Cingulate Gyrus	brain
16	chr8:20958600-20959600	Weak transcription	Right Atrium	heart

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