Variant report

Variant	rs56158089
Chromosome Location	chr7:150278547-150278548
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	chr7:150232590..150235233-chr7:150277857..150280710,2	K562	blood:

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10085891	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10216102	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10224387	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10227094	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10232947	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10239578	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10240209	0.80[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10248553	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10255487	0.80[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10270122	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10273606	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11971770	0.92[EUR][1000 genomes]
rs11975418	0.85[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11984138	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12671922	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1317276	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1916027	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2140138	0.92[EUR][1000 genomes]
rs2140139	0.92[EUR][1000 genomes]
rs2140145	0.83[EUR][1000 genomes]
rs28537284	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28829297	0.82[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4143732	0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs55653011	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs57604196	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs60628216	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6464081	0.92[EUR][1000 genomes]
rs6959171	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6959264	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6961075	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs73727323	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs73727325	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs73727338	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7781704	0.89[EUR][1000 genomes]
rs7782221	0.92[EUR][1000 genomes]
rs7787987	0.92[EUR][1000 genomes]
rs7797456	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7800143	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7802869	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7806724	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs952642	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9640279	0.92[AMR][1000 genomes];0.95[EUR][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	nsv1034409	chr7:149844639-150447071	Flanking Active TSS Active TSS Genic enhancers Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription Strong transcription 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	75 gene(s)	inside rSNPs	diseases
2	nsv608990	chr7:149961274-150707488	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
3	nsv1015582	chr7:149967986-150285104	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
4	nsv1017368	chr7:150016952-150655773	Bivalent Enhancer ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
5	nsv539195	chr7:150016952-150655773	Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
6	esv3395746	chr7:150181141-150300680	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
7	esv16529	chr7:150249312-150312843	Genic enhancers Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
8	esv2758617	chr7:150251949-150463804	Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Enhancers ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
9	esv2759573	chr7:150251949-150463804	Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:150269800-150282400	Weak transcription	Right Ventricle	heart
2	chr7:150270200-150281800	Weak transcription	Spleen	Spleen
3	chr7:150275000-150278600	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr7:150276600-150278600	Enhancers	Primary neutrophils fromperipheralblood	blood
5	chr7:150276800-150278600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr7:150277200-150278600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr7:150277600-150278800	Enhancers	Primary hematopoietic stem cells	blood
8	chr7:150277600-150281200	ZNF genes & repeats	Primary T cells from cord blood	blood
9	chr7:150277800-150279000	ZNF genes & repeats	Liver	Liver
10	chr7:150277800-150280200	ZNF genes & repeats	Primary T helper naive cells fromperipheralblood	blood
11	chr7:150278000-150279600	ZNF genes & repeats	Primary T regulatory cells fromperipheralblood	blood
12	chr7:150278200-150278600	ZNF genes & repeats	Primary B cells from cord blood	blood
13	chr7:150278400-150278600	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
14	chr7:150278400-150279000	Enhancers	GM12878-XiMat	blood
15	chr7:150278400-150283400	Weak transcription	Primary hematopoietic stem cells short term culture	blood

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