Variant report

Variant	rs1446041
Chromosome Location	chr5:15072948-15072949
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs10475041	1.00[ASN][1000 genomes]
rs11741614	1.00[ASN][1000 genomes]
rs11750471	1.00[ASN][1000 genomes]
rs1502037	1.00[ASN][1000 genomes]
rs1502038	1.00[ASN][1000 genomes]
rs16903776	1.00[ASN][1000 genomes]
rs16903801	0.92[AFR][1000 genomes]
rs17342417	1.00[ASN][1000 genomes]
rs2455490	1.00[ASN][1000 genomes]
rs251538	1.00[ASN][1000 genomes]
rs2652759	1.00[ASN][1000 genomes]
rs2652761	1.00[ASN][1000 genomes]
rs28287	1.00[ASN][1000 genomes]
rs301080	1.00[ASN][1000 genomes]
rs32440	1.00[ASN][1000 genomes]
rs32443	0.85[MEX][hapmap]
rs32444	0.93[CEU][hapmap]
rs32445	1.00[ASN][1000 genomes]
rs32446	0.86[MEX][hapmap]
rs32448	0.86[MEX][hapmap]
rs32451	1.00[ASN][1000 genomes]
rs32452	1.00[CEU][hapmap];1.00[ASN][1000 genomes]
rs32453	1.00[ASN][1000 genomes]
rs32454	1.00[ASN][1000 genomes]
rs32455	1.00[ASN][1000 genomes]
rs32456	0.82[ASW][hapmap];1.00[CEU][hapmap];1.00[CHD][hapmap];0.88[GIH][hapmap];1.00[MEX][hapmap];0.87[MKK][hapmap];1.00[ASN][1000 genomes]
rs32463	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs32464	1.00[ASN][1000 genomes]
rs32466	1.00[ASN][1000 genomes]
rs32467	0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs62356079	1.00[ASN][1000 genomes]
rs62356080	1.00[ASN][1000 genomes]
rs62356081	1.00[ASN][1000 genomes]
rs62356082	1.00[ASN][1000 genomes]
rs6866660	1.00[ASN][1000 genomes]
rs6868543	1.00[ASN][1000 genomes]
rs6873180	1.00[ASN][1000 genomes]
rs6888138	1.00[ASN][1000 genomes]
rs7341022	0.81[TSI][hapmap]
rs7708423	1.00[ASN][1000 genomes]
rs7708528	1.00[ASN][1000 genomes]
rs7727179	1.00[ASN][1000 genomes]
rs836147	1.00[ASN][1000 genomes]
rs836148	1.00[ASN][1000 genomes]
rs836149	1.00[ASN][1000 genomes]
rs856751	1.00[ASN][1000 genomes]
rs863162	1.00[ASN][1000 genomes]
rs9687484	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	nsv1018187	chr5:14385164-15127103	Strong transcription Flanking Bivalent TSS/Enh Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
2	nsv530221	chr5:14859687-15364470	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
3	nsv432717	chr5:14887400-15126500	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
4	nsv1017579	chr5:14888997-15194335	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:15070000-15074800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr5:15070600-15074600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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