Variant report

Variant	rs17152532
Chromosome Location	chr5:124605395-124605396
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs11740444	0.82[ASN][1000 genomes]
rs13157669	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13162906	0.91[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs13172476	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13177664	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13185858	0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1347924	0.87[ASN][1000 genomes]
rs1439581	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17152498	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17152511	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17152519	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17152524	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17152545	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17152569	0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17152577	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17152579	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2408379	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34833831	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34892968	0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs35073242	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35108894	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35654224	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35802525	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35914668	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36050183	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6595603	0.87[ASN][1000 genomes]
rs6892733	0.87[ASN][1000 genomes]
rs73311010	0.82[ASN][1000 genomes]
rs7721989	0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv882823	chr5:124569471-124639468	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:124593200-124609200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr5:124599600-124608600	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr5:124599600-124608600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr5:124599800-124613400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr5:124603800-124605400	Weak transcription	Stomach Mucosa	stomach
6	chr5:124604200-124612400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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