Variant report

Variant	rs2479787
Chromosome Location	chr13:29655506-29655507
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:29654983..29655766-chr13:29834963..29835491,2	MCF-7	breast:
2	chr13:29654937..29655772-chr13:29936880..29937545,2	MCF-7	breast:

Extended variants
information (count: 67 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:65)

rs_ID	r²[population]
rs1006810	0.82[JPT][hapmap]
rs11620188	0.81[JPT][hapmap]
rs12858770	0.88[ASN][1000 genomes]
rs1322383	0.89[ASN][1000 genomes]
rs1322385	0.80[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs1590277	0.90[JPT][hapmap]
rs167833	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs184467	0.86[ASN][1000 genomes]
rs187333	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs191265	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2077255	0.96[CEU][hapmap];0.83[CHB][hapmap];0.90[JPT][hapmap]
rs2146139	0.89[ASN][1000 genomes]
rs2146140	0.89[ASN][1000 genomes]
rs2181182	0.94[CHB][hapmap];0.90[JPT][hapmap];0.89[ASN][1000 genomes]
rs2181183	0.89[ASN][1000 genomes]
rs2475512	0.88[ASN][1000 genomes]
rs2475514	0.89[ASN][1000 genomes]
rs2475515	0.94[CHB][hapmap];0.91[JPT][hapmap];0.89[ASN][1000 genomes]
rs2475518	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2475519	0.94[CHB][hapmap];0.91[JPT][hapmap];0.89[ASN][1000 genomes]
rs2475520	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2475523	0.89[ASN][1000 genomes]
rs2475524	0.94[CHB][hapmap];0.91[JPT][hapmap];0.89[ASN][1000 genomes]
rs2475525	0.89[ASN][1000 genomes]
rs2475537	0.81[JPT][hapmap]
rs2475546	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2475548	1.00[CEU][hapmap];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2475550	0.94[CHB][hapmap];0.91[JPT][hapmap];0.89[ASN][1000 genomes]
rs2475551	0.94[CHB][hapmap];0.91[JPT][hapmap];0.89[ASN][1000 genomes]
rs2479778	0.94[CHB][hapmap];0.91[JPT][hapmap];0.89[ASN][1000 genomes]
rs2479779	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2479781	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2479785	0.89[ASN][1000 genomes]
rs2479786	0.94[CHB][hapmap];0.91[JPT][hapmap];0.89[ASN][1000 genomes]
rs2987344	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs326513	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs326514	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs326515	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs326517	0.96[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs326524	0.94[CHB][hapmap];0.90[JPT][hapmap];0.87[ASN][1000 genomes]
rs326526	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4262810	0.88[ASN][1000 genomes]
rs4769676	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6490346	0.96[CEU][hapmap];0.84[CHB][hapmap];0.91[JPT][hapmap]
rs7317087	0.92[CEU][hapmap];0.84[CHB][hapmap];0.95[JPT][hapmap];0.80[ASN][1000 genomes]
rs7326464	0.92[CEU][hapmap];0.83[CHB][hapmap];0.90[JPT][hapmap]
rs7328602	0.96[CEU][hapmap];0.84[CHB][hapmap];0.91[JPT][hapmap]
rs7332330	0.96[CEU][hapmap];0.84[CHB][hapmap];0.95[JPT][hapmap];0.81[YRI][hapmap]
rs7334030	0.80[ASN][1000 genomes]
rs7337190	0.92[CEU][hapmap];0.83[CHB][hapmap];0.90[JPT][hapmap]
rs7339409	0.93[CEU][hapmap];0.84[CHB][hapmap];0.91[JPT][hapmap];0.87[YRI][hapmap];0.80[ASN][1000 genomes]
rs745423	0.96[CEU][hapmap];0.83[CHB][hapmap];0.90[JPT][hapmap]
rs754395	0.96[CEU][hapmap];0.83[CHB][hapmap];0.90[JPT][hapmap]
rs7986144	0.83[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs913494	0.96[CEU][hapmap];0.83[CHB][hapmap];0.90[JPT][hapmap]
rs9314927	0.86[JPT][hapmap]
rs9506080	0.83[JPT][hapmap]
rs9506089	0.89[ASN][1000 genomes]
rs9508235	0.96[CEU][hapmap];0.84[CHB][hapmap];0.90[JPT][hapmap]
rs9550435	0.82[JPT][hapmap]
rs9550437	0.82[JPT][hapmap]
rs9551598	0.83[JPT][hapmap]
rs9578072	0.94[CHB][hapmap];0.91[JPT][hapmap]
rs9579284	0.90[JPT][hapmap]
rs9579290	0.86[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533835	chr13:29141132-29962069	Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
2	esv3406145	chr13:29616606-29917459	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 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	chr13:29654600-29656600	Enhancers	Primary B cells from peripheral blood	blood
2	chr13:29654600-29657000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
3	chr13:29654600-29657600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
4	chr13:29654800-29656400	Enhancers	Primary B cells from cord blood	blood
5	chr13:29655000-29655800	Enhancers	GM12878-XiMat	blood
6	chr13:29655000-29656400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
7	chr13:29655000-29656400	Enhancers	Primary T helper cells fromperipheralblood	blood
8	chr13:29655000-29656800	Enhancers	Dnd41	blood
9	chr13:29655000-29657600	Enhancers	Fetal Heart	heart
10	chr13:29655200-29656200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
11	chr13:29655400-29655800	Flanking Active TSS	Primary T cells from cord blood	blood
12	chr13:29655400-29655800	Weak transcription	Primary T cells fromperipheralblood	blood
13	chr13:29655400-29656200	Weak transcription	Aorta	Aorta
14	chr13:29655400-29656600	Enhancers	Primary T helper cells PMA-I stimulated	--

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