Variant report

Variant	rs16969491
Chromosome Location	chr15:39939583-39939584
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:39934745..39936337-chr15:39938200..39940638,2	MCF-7	breast:

Extended variants
information (count: 84 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:77)

rs_ID	r²[population]
rs10152903	1.00[CHB][hapmap]
rs10152951	1.00[CHB][hapmap]
rs1038097	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1051442	0.86[CEU][hapmap];1.00[CHB][hapmap];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10520141	0.86[CEU][hapmap];1.00[CHB][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10520143	0.88[CEU][hapmap];1.00[CHB][hapmap];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10520145	1.00[CHB][hapmap]
rs10520146	1.00[CHB][hapmap];0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10520147	1.00[CHB][hapmap]
rs10520148	1.00[CHB][hapmap]
rs1073675	1.00[CHB][hapmap]
rs1382443	0.86[CEU][hapmap];1.00[CHB][hapmap];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1382444	0.86[CEU][hapmap];1.00[CHB][hapmap];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs16969167	1.00[CHB][hapmap]
rs16969487	0.88[CEU][hapmap];1.00[CHB][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs16969547	1.00[CHB][hapmap];0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs16969663	1.00[CHB][hapmap]
rs16969664	1.00[CHB][hapmap]
rs16969666	1.00[CHB][hapmap]
rs16969672	1.00[CHB][hapmap]
rs16969679	1.00[CHB][hapmap]
rs16969680	1.00[CHB][hapmap]
rs16969688	1.00[CHB][hapmap]
rs17632916	0.88[CEU][hapmap];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs17633107	0.88[CEU][hapmap];1.00[CHB][hapmap];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs17633210	0.86[CEU][hapmap];1.00[CHB][hapmap];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs17705806	0.88[CEU][hapmap];1.00[CHB][hapmap];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs17706083	0.86[CEU][hapmap];1.00[CHB][hapmap];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs17706179	0.88[CEU][hapmap];1.00[CHB][hapmap];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs17717859	1.00[CHB][hapmap]
rs1813493	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1988082	0.81[EUR][1000 genomes]
rs1988555	0.85[EUR][1000 genomes]
rs1994380	1.00[CHB][hapmap]
rs2129457	1.00[CHB][hapmap]
rs2228262	1.00[CHB][hapmap]
rs2228263	0.86[CEU][hapmap];1.00[CHB][hapmap];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2411316	0.88[CEU][hapmap];1.00[CHB][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2618156	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2618160	0.90[EUR][1000 genomes]
rs2618161	0.86[CEU][hapmap];1.00[CHB][hapmap];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2618164	0.86[CEU][hapmap];0.91[EUR][1000 genomes]
rs2618165	0.88[CEU][hapmap];0.91[EUR][1000 genomes]
rs2618167	0.88[CEU][hapmap];1.00[CHB][hapmap];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2664123	0.90[EUR][1000 genomes]
rs2664136	0.91[EUR][1000 genomes]
rs2664137	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2664138	1.00[CHB][hapmap];0.89[EUR][1000 genomes]
rs2664140	0.90[EUR][1000 genomes]
rs2664142	0.90[EUR][1000 genomes]
rs28377784	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs28549326	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs28619289	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs28653011	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs34878675	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs41315060	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4415979	0.86[CEU][hapmap];1.00[CHB][hapmap];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4503768	0.88[CEU][hapmap];1.00[CHB][hapmap];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs45461294	0.94[EUR][1000 genomes]
rs4923835	1.00[CHB][hapmap];0.85[EUR][1000 genomes]
rs58188999	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs59578395	0.80[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs59628570	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6492905	0.86[CEU][hapmap];1.00[CHB][hapmap];0.93[EUR][1000 genomes]
rs7172155	1.00[CHB][hapmap]
rs7173948	1.00[CHB][hapmap]
rs7179604	1.00[CHB][hapmap]
rs7181354	1.00[CHB][hapmap]
rs7182423	1.00[CHB][hapmap]
rs74008647	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs74008648	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs8041266	1.00[CHB][hapmap]
rs880270	0.88[CEU][hapmap];1.00[CHB][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs937961	1.00[CHB][hapmap]
rs937962	1.00[CHB][hapmap]
rs954152	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9972350	0.86[CEU][hapmap];1.00[CHB][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1049682	chr15:39657279-40027403	Enhancers Flanking Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv542361	chr15:39657279-40027403	Weak transcription Strong transcription Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
3	esv3373125	chr15:39691567-40061262	Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
4	nsv904094	chr15:39738006-39976057	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
5	nsv832977	chr15:39817512-39981520	Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
6	nsv1048628	chr15:39877498-39940104	Enhancers Genic enhancers Strong transcription ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
7	nsv832978	chr15:39899759-40094881	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:39923800-39939600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr15:39937000-39941200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
3	chr15:39937800-39943200	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr15:39938000-39944400	Weak transcription	HSMMtube	muscle
5	chr15:39938000-39950000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr15:39938000-39957600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr15:39938200-39950800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr15:39938400-39941800	Weak transcription	Left Ventricle	heart

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