Variant report

Variant	rs1344612
Chromosome Location	chr4:95265228-95265229
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 70 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:67)

rs_ID	r²[population]
rs10006191	0.83[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs10020236	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10856909	0.99[ASN][1000 genomes]
rs11097414	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11097417	0.99[ASN][1000 genomes]
rs11097418	0.84[ASN][1000 genomes]
rs11727030	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11932054	0.84[ASN][1000 genomes]
rs12507134	0.86[ASN][1000 genomes]
rs12646487	0.85[ASN][1000 genomes]
rs12646673	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs13138688	0.80[EUR][1000 genomes]
rs13146089	0.85[ASN][1000 genomes]
rs1426575	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1593553	0.84[EUR][1000 genomes]
rs1593554	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17021507	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17021531	0.85[ASN][1000 genomes]
rs17311008	0.94[ASN][1000 genomes]
rs17377118	0.86[ASN][1000 genomes]
rs17565759	0.86[ASN][1000 genomes]
rs1965049	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1965696	0.94[ASN][1000 genomes]
rs1991316	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2016476	0.82[EUR][1000 genomes]
rs2059605	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2195001	0.85[ASN][1000 genomes]
rs2289186	0.84[EUR][1000 genomes]
rs28408371	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs28437833	0.85[ASN][1000 genomes]
rs2865353	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs34181160	0.94[ASN][1000 genomes]
rs3919616	0.85[ASN][1000 genomes]
rs4282187	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs57939388	0.86[ASN][1000 genomes]
rs58796749	0.93[ASN][1000 genomes]
rs59483091	0.87[ASN][1000 genomes]
rs61056400	0.85[ASN][1000 genomes]
rs62320441	0.90[ASN][1000 genomes]
rs62320444	0.92[ASN][1000 genomes]
rs6419132	0.84[ASN][1000 genomes]
rs6532479	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6532480	0.87[ASN][1000 genomes]
rs6532481	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6532482	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6825005	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6826671	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6839224	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6839950	0.85[ASN][1000 genomes]
rs6840409	0.85[ASN][1000 genomes]
rs6840479	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6847767	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6847989	0.87[ASN][1000 genomes]
rs6851128	0.96[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs724260	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7438414	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7657805	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7666873	0.85[ASN][1000 genomes]
rs7670194	0.85[ASN][1000 genomes]
rs7672156	0.84[ASN][1000 genomes]
rs7672464	0.98[ASN][1000 genomes]
rs7672527	0.99[ASN][1000 genomes]
rs7672999	0.94[ASN][1000 genomes]
rs7691132	0.84[ASN][1000 genomes]
rs7694491	0.84[ASN][1000 genomes]
rs901615	0.82[EUR][1000 genomes]
rs9997915	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv993495	chr4:94992315-95482578	Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
2	nsv594901	chr4:95254730-95493246	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
3	nsv1003743	chr4:95255957-95469831	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:95260400-95266400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr4:95261400-95271400	Weak transcription	Dnd41	blood
3	chr4:95263200-95266600	Weak transcription	Adipose Nuclei	Adipose
4	chr4:95263800-95265400	Weak transcription	Placenta	Placenta
5	chr4:95264200-95266400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr4:95264200-95266400	Weak transcription	GM12878-XiMat	blood
7	chr4:95264400-95265600	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr4:95264400-95266400	Weak transcription	K562	blood
9	chr4:95264400-95268600	Enhancers	Primary hematopoietic stem cells	blood
10	chr4:95264400-95268600	Enhancers	Primary hematopoietic stem cells short term culture	blood
11	chr4:95264600-95265800	Weak transcription	Monocytes-CD14+_RO01746	blood
12	chr4:95264600-95266400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr4:95264600-95267800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr4:95265200-95266600	Enhancers	Primary monocytes fromperipheralblood	blood

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