Variant report

Variant	rs74089148
Chromosome Location	chr14:104510745-104510746
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs11849381	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11852063	1.00[AMR][1000 genomes]
rs56687774	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59108783	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60710970	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7146464	1.00[AMR][1000 genomes]
rs73356331	1.00[AMR][1000 genomes]
rs74086986	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74086988	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74087001	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74087002	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74089115	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74089126	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74089150	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74089153	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74089170	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74089177	0.94[AFR][1000 genomes]
rs8014686	1.00[AMR][1000 genomes]
rs8014751	1.00[AMR][1000 genomes]
rs9324065	1.00[AMR][1000 genomes]
rs9671937	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1045162	chr14:104140525-104594841	Flanking Active TSS Strong transcription Bivalent Enhancer Enhancers Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
2	nsv542204	chr14:104140525-104594841	Active TSS Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
3	nsv902319	chr14:104255083-104620077	Weak transcription Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	64 gene(s)	inside rSNPs	diseases
4	nsv1049690	chr14:104411621-104575838	Enhancers ZNF genes & repeats Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
5	nsv542208	chr14:104411621-104575838	Enhancers ZNF genes & repeats Genic enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
6	nsv526680	chr14:104427043-104568472	Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
7	nsv1047990	chr14:104460605-104556463	Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
8	nsv542209	chr14:104497447-104540729	Bivalent Enhancer ZNF genes & repeats Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
9	nsv1050479	chr14:104500427-104805738	Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:104492200-104516000	Weak transcription	Spleen	Spleen
2	chr14:104496400-104520800	Weak transcription	Primary monocytes fromperipheralblood	blood
3	chr14:104499000-104511800	Strong transcription	Monocytes-CD14+_RO01746	blood
4	chr14:104502800-104513400	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr14:104509200-104520600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr14:104510000-104510800	Strong transcription	Primary neutrophils fromperipheralblood	blood
7	chr14:104510200-104511000	Enhancers	Muscle Satellite Cultured Cells	--
8	chr14:104510600-104516200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood

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