Variant report

Variant	rs984164
Chromosome Location	chr5:35908015-35908016
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs1008756	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1010599	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1010601	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1025039	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10491434	1.00[JPT][hapmap]
rs1053496	1.00[JPT][hapmap]
rs11567699	1.00[JPT][hapmap]
rs11567701	1.00[JPT][hapmap]
rs11567751	1.00[JPT][hapmap]
rs11949691	1.00[ASN][1000 genomes]
rs11955657	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1345827	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1382347	1.00[JPT][hapmap]
rs1494554	1.00[JPT][hapmap]
rs1494571	1.00[JPT][hapmap]
rs16902573	1.00[ASN][1000 genomes]
rs17376481	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];1.00[TSI][hapmap];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1833907	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2194224	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2287900	1.00[ASN][1000 genomes]
rs2361403	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3194051	1.00[JPT][hapmap]
rs3734107	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs3822733	1.00[JPT][hapmap]
rs4024109	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4024110	0.83[ASN][1000 genomes]
rs55654952	0.97[ASN][1000 genomes]
rs59030624	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6859465	0.89[ASN][1000 genomes]
rs6862692	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6871116	1.00[JPT][hapmap]
rs6873195	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6878577	0.82[AFR][1000 genomes];0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6878688	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs700179	1.00[JPT][hapmap]
rs72742471	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7702587	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7702828	0.94[ASN][1000 genomes]
rs7705615	1.00[ASN][1000 genomes]
rs7716969	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7719334	0.83[AFR][1000 genomes];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7723452	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs852242	0.89[CEU][hapmap]
rs852249	1.00[ASW][hapmap];0.91[LWK][hapmap];0.87[MKK][hapmap];0.84[YRI][hapmap]
rs852250	1.00[ASW][hapmap];0.91[LWK][hapmap];0.87[MKK][hapmap];0.84[YRI][hapmap]
rs9764914	0.89[ASN][1000 genomes]
rs9765078	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs987107	1.00[JPT][hapmap]
rs990716	1.00[CHB][hapmap];0.85[CHD][hapmap];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv471011	chr5:35861068-36003217	Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS Active TSS Genic enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv830261	chr5:35863084-36018048	Weak transcription ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv1025695	chr5:35902486-36036934	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv4794	chr5:35906690-35934205	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	4 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	chr5:35899000-35909200	Enhancers	Fetal Thymus	thymus
2	chr5:35905000-35908200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
3	chr5:35905000-35908400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
4	chr5:35905200-35908800	Enhancers	Dnd41	blood
5	chr5:35905400-35908400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
6	chr5:35905400-35908800	Weak transcription	Primary T helper cells fromperipheralblood	blood
7	chr5:35906000-35908200	Weak transcription	Primary T helper cells PMA-I stimulated	--
8	chr5:35906000-35908400	Weak transcription	GM12878-XiMat	blood
9	chr5:35907600-35909400	Enhancers	Thymus	Thymus
10	chr5:35907600-35909600	Enhancers	Primary hematopoietic stem cells	blood
11	chr5:35907800-35909600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr5:35907800-35910000	Enhancers	Primary hematopoietic stem cells short term culture	blood
13	chr5:35908000-35908400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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