Variant report

Variant	rs4725923
Chromosome Location	chr7:150278849-150278850
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: 70 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:61)

rs_ID	r²[population]
rs1110093	0.88[EUR][1000 genomes]
rs11760959	0.88[EUR][1000 genomes]
rs11760960	0.88[EUR][1000 genomes]
rs11761391	0.85[EUR][1000 genomes]
rs11763828	0.86[JPT][hapmap]
rs11765395	0.88[EUR][1000 genomes]
rs11768988	0.88[EUR][1000 genomes]
rs11769223	0.88[EUR][1000 genomes]
rs11770957	0.88[EUR][1000 genomes]
rs11771561	0.91[EUR][1000 genomes]
rs11771962	0.81[EUR][1000 genomes]
rs11772952	0.88[EUR][1000 genomes]
rs11982681	0.87[EUR][1000 genomes]
rs12672072	0.87[EUR][1000 genomes]
rs12703078	0.85[EUR][1000 genomes]
rs12703083	0.90[EUR][1000 genomes]
rs13222905	0.90[EUR][1000 genomes]
rs13224067	0.88[EUR][1000 genomes]
rs13231883	0.90[EUR][1000 genomes]
rs13232597	0.90[EUR][1000 genomes]
rs13240941	0.87[EUR][1000 genomes]
rs13242186	0.90[EUR][1000 genomes]
rs1568629	0.85[EUR][1000 genomes]
rs1916003	0.87[EUR][1000 genomes]
rs2177188	0.89[EUR][1000 genomes]
rs2293172	0.93[EUR][1000 genomes]
rs2293174	0.91[EUR][1000 genomes]
rs2373802	0.81[EUR][1000 genomes]
rs2373815	0.90[EUR][1000 genomes]
rs34211617	0.88[EUR][1000 genomes]
rs34514106	0.87[EUR][1000 genomes]
rs34545650	0.94[EUR][1000 genomes]
rs35133885	0.87[EUR][1000 genomes]
rs35194540	0.88[EUR][1000 genomes]
rs35225135	0.85[EUR][1000 genomes]
rs35388682	0.88[EUR][1000 genomes]
rs35496043	0.88[EUR][1000 genomes]
rs35556724	0.86[EUR][1000 genomes]
rs35672177	0.87[EUR][1000 genomes]
rs35677477	0.88[EUR][1000 genomes]
rs36021964	0.87[EUR][1000 genomes]
rs36185661	0.90[EUR][1000 genomes]
rs3807378	0.92[EUR][1000 genomes]
rs4725345	0.88[EUR][1000 genomes]
rs4725348	0.86[EUR][1000 genomes]
rs4725908	0.87[EUR][1000 genomes]
rs4725921	0.93[EUR][1000 genomes]
rs58414124	0.87[EUR][1000 genomes]
rs62502270	0.91[EUR][1000 genomes]
rs62503177	0.87[EUR][1000 genomes]
rs6464083	0.80[JPT][hapmap]
rs6949485	0.87[EUR][1000 genomes]
rs6959610	0.80[JPT][hapmap]
rs6963908	0.80[JPT][hapmap]
rs6969136	0.80[JPT][hapmap]
rs6969847	0.80[JPT][hapmap]
rs73163503	0.91[EUR][1000 genomes]
rs7782113	0.87[EUR][1000 genomes]
rs7802853	0.87[EUR][1000 genomes]
rs7803234	0.87[EUR][1000 genomes]
rs7809438	0.87[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:13 , 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	chr7:150277600-150281200	ZNF genes & repeats	Primary T cells from cord blood	blood
4	chr7:150277800-150279000	ZNF genes & repeats	Liver	Liver
5	chr7:150277800-150280200	ZNF genes & repeats	Primary T helper naive cells fromperipheralblood	blood
6	chr7:150278000-150279600	ZNF genes & repeats	Primary T regulatory cells fromperipheralblood	blood
7	chr7:150278400-150279000	Enhancers	GM12878-XiMat	blood
8	chr7:150278400-150283400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
9	chr7:150278600-150279800	Weak transcription	Monocytes-CD14+_RO01746	blood
10	chr7:150278600-150283000	Weak transcription	Primary neutrophils fromperipheralblood	blood
11	chr7:150278600-150283200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr7:150278600-150283400	Weak transcription	Primary B cells from cord blood	blood
13	chr7:150278800-150283000	Weak transcription	Primary hematopoietic stem cells	blood

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