Variant report

Variant	rs17667157
Chromosome Location	chr10:26487498-26487499
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	NFYB	chr10:26487420-26487620	GM12878	blood:	n/a	n/a

Variant related genes	Relation type
MYO3A	TF binding region

Extended variants
information (count: 79 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:78)

rs_ID	r²[population]
rs10508713	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11812152	1.00[CHB][hapmap]
rs11812332	1.00[CHB][hapmap]
rs11812370	0.88[CEU][hapmap];1.00[CHB][hapmap];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11812543	1.00[CHB][hapmap]
rs11813728	1.00[CHB][hapmap]
rs11815755	1.00[CEU][hapmap];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11816461	1.00[ASW][hapmap];0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[MEX][hapmap];0.89[MKK][hapmap];0.89[TSI][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11816664	0.92[AMR][1000 genomes]
rs11817896	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11818977	1.00[CHB][hapmap]
rs11819181	1.00[CHB][hapmap]
rs11819744	1.00[CHB][hapmap]
rs1521037	1.00[CHB][hapmap]
rs1521038	1.00[CHB][hapmap]
rs16926590	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[MEX][hapmap];0.89[TSI][hapmap];0.92[AMR][1000 genomes]
rs16926628	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[MEX][hapmap];0.85[TSI][hapmap];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs16926660	1.00[MEX][hapmap];0.89[TSI][hapmap];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs16926667	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17666132	1.00[CHB][hapmap]
rs17666138	1.00[CHB][hapmap]
rs17666263	1.00[CHB][hapmap]
rs17666893	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs17738738	1.00[CHB][hapmap]
rs17738768	1.00[CHB][hapmap]
rs17738883	1.00[CHB][hapmap]
rs17738907	1.00[CHB][hapmap]
rs17738949	1.00[CHB][hapmap]
rs17739436	1.00[ASW][hapmap];0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[MEX][hapmap];0.83[MKK][hapmap];0.85[TSI][hapmap];1.00[YRI][hapmap];0.96[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17739453	1.00[ASW][hapmap];0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[MEX][hapmap];0.89[MKK][hapmap];0.89[TSI][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17739680	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1935485	1.00[CHB][hapmap]
rs2222351	0.92[AMR][1000 genomes]
rs3897758	0.96[AMR][1000 genomes]
rs41279908	0.81[AFR][1000 genomes];0.96[AMR][1000 genomes]
rs41454449	1.00[CHB][hapmap]
rs4370835	0.82[CEU][hapmap];1.00[CHB][hapmap];0.96[AMR][1000 genomes]
rs56153367	0.96[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56234810	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57140603	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57687518	0.92[AMR][1000 genomes]
rs58309865	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs58990448	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59646929	0.96[AMR][1000 genomes]
rs61284099	0.96[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6650135	1.00[CHB][hapmap];1.00[MEX][hapmap];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7074143	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7082557	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs72787349	0.81[AFR][1000 genomes];0.96[AMR][1000 genomes]
rs72787350	0.96[AMR][1000 genomes]
rs72789947	0.92[AMR][1000 genomes]
rs72789954	0.96[AMR][1000 genomes]
rs72789957	0.92[AMR][1000 genomes]
rs72789960	0.92[AMR][1000 genomes]
rs72793209	0.96[AMR][1000 genomes]
rs72793210	0.96[AMR][1000 genomes]
rs72793214	0.96[AMR][1000 genomes]
rs72793215	0.92[AMR][1000 genomes]
rs72793218	0.92[AMR][1000 genomes]
rs72793939	0.88[AMR][1000 genomes]
rs72793940	0.96[AMR][1000 genomes]
rs72793945	0.92[AMR][1000 genomes]
rs72793992	0.96[AMR][1000 genomes]
rs74126361	0.96[AMR][1000 genomes]
rs74126386	0.92[AMR][1000 genomes]
rs74126397	0.81[AFR][1000 genomes];0.96[AMR][1000 genomes]
rs74126400	0.92[AMR][1000 genomes]
rs74126401	0.92[AMR][1000 genomes]
rs74126402	0.81[AFR][1000 genomes];0.96[AMR][1000 genomes]
rs74129103	0.92[AMR][1000 genomes]
rs74129107	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74129109	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs74129112	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74129113	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7476089	1.00[CHB][hapmap]
rs7894269	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[MEX][hapmap];0.85[TSI][hapmap];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7909349	1.00[ASW][hapmap];0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[MEX][hapmap];0.89[MKK][hapmap];0.89[TSI][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7919609	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.89[EUR][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	nsv894975	chr10:26343356-27014467	Strong transcription Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:26474000-26491000	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr10:26483200-26489000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr10:26483600-26488600	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr10:26484800-26493400	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr10:26486600-26493800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr10:26487400-26487600	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr10:26487400-26489600	Enhancers	ES-I3 Cell Line	embryonic stem cell

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