Variant report

Variant	rs6898899
Chromosome Location	chr5:126931374-126931375
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs34236997	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3756723	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs55654285	1.00[ASN][1000 genomes]
rs55749092	1.00[ASN][1000 genomes]
rs57117879	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58380010	1.00[ASN][1000 genomes]
rs60285859	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60654462	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61220586	1.00[ASN][1000 genomes]
rs6875028	1.00[ASN][1000 genomes]
rs6884394	1.00[MEX][hapmap]
rs6885226	1.00[MEX][hapmap]
rs6893537	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6893841	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6893881	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6894854	1.00[ASN][1000 genomes]
rs73335069	0.95[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73335075	0.92[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73335078	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73335089	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73335092	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73783908	1.00[ASN][1000 genomes]
rs73783909	1.00[ASN][1000 genomes]
rs73783910	1.00[ASN][1000 genomes]
rs73783911	1.00[ASN][1000 genomes]
rs73783912	1.00[ASN][1000 genomes]
rs73783913	1.00[ASN][1000 genomes]
rs73783914	1.00[ASN][1000 genomes]
rs73783917	1.00[ASN][1000 genomes]
rs73783918	1.00[ASN][1000 genomes]
rs73783922	1.00[ASN][1000 genomes]
rs73783923	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73783924	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73783925	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7705105	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7710290	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7715074	1.00[ASN][1000 genomes]
rs7723932	1.00[ASN][1000 genomes]
rs7735444	0.85[AMR][1000 genomes]
rs7737835	1.00[MEX][hapmap]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1033607	chr5:126385181-127304459	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
2	nsv1019821	chr5:126658200-126934917	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv537894	chr5:126658200-126934917	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv830478	chr5:126721368-126937408	Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
5	nsv830479	chr5:126849254-127053121	Genic enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
6	nsv1021483	chr5:126927834-127304873	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 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	chr5:126921400-126936600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr5:126922200-126939200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr5:126926200-126931600	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr5:126926400-126931600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr5:126930000-126931400	Enhancers	Thymus	Thymus
6	chr5:126930000-126933200	Enhancers	Primary T cells from cord blood	blood
7	chr5:126930600-126933400	Enhancers	Fetal Thymus	thymus
8	chr5:126930800-126931600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
9	chr5:126930800-126931800	Enhancers	Primary T helper cells PMA-I stimulated	--
10	chr5:126931000-126931800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
11	chr5:126931200-126931400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr5:126931200-126931400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr5:126931200-126931600	Enhancers	Primary T cells fromperipheralblood	blood

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