Variant report

Variant	rs11014976
Chromosome Location	chr10:26450959-26450960
allele	C/T
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	MAFK	chr10:26450905-26451017	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr10:26450922-26451049	H1-hESC	embryonic stem cell:	n/a	n/a
3	MAX	chr10:26450695-26451024	H1-hESC	embryonic stem cell:	n/a	n/a

Variant related genes	Relation type
MYO3A	TF binding region

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs10508714	0.89[JPT][hapmap];0.85[ASN][1000 genomes]
rs10764598	1.00[ASN][1000 genomes]
rs10828955	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11014959	0.95[CEU][hapmap];0.95[EUR][1000 genomes]
rs11014979	1.00[ASN][1000 genomes]
rs11014984	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs11593041	1.00[ASN][1000 genomes]
rs12247347	0.81[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs12247680	0.95[EUR][1000 genomes]
rs12258401	1.00[ASN][1000 genomes]
rs12258453	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12261502	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs12262728	1.00[ASN][1000 genomes]
rs12266309	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12267078	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs12411554	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12569739	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs12765561	0.85[CEU][hapmap]
rs12774270	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs1342319	0.91[ASN][1000 genomes]
rs1342320	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs1539323	0.93[EUR][1000 genomes]
rs17739425	1.00[CEU][hapmap];0.87[YRI][hapmap];0.96[EUR][1000 genomes]
rs1818747	0.94[EUR][1000 genomes]
rs1935484	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2096176	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.95[YRI][hapmap];0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2226129	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2368157	1.00[CEU][hapmap];0.98[EUR][1000 genomes]
rs2368158	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.95[YRI][hapmap];0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3740231	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3740232	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs3758447	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3758448	1.00[ASN][1000 genomes]
rs3758449	0.90[CHB][hapmap];0.94[JPT][hapmap];0.93[ASN][1000 genomes]
rs4539209	1.00[ASN][1000 genomes]
rs4575167	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs61840836	0.95[EUR][1000 genomes]
rs6482531	0.90[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs6482532	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7072451	1.00[ASN][1000 genomes]
rs7079125	0.92[ASN][1000 genomes]
rs7079780	0.93[ASN][1000 genomes]
rs7080516	0.96[EUR][1000 genomes]
rs7081905	1.00[CHB][hapmap];0.94[JPT][hapmap];0.95[ASN][1000 genomes]
rs7082411	0.91[ASN][1000 genomes]
rs7084000	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7085103	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.95[YRI][hapmap];0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7091566	0.91[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.95[YRI][hapmap];0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7093989	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.95[YRI][hapmap];0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7095559	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs7096646	0.95[ASN][1000 genomes]
rs7476324	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs7898544	0.96[CEU][hapmap];0.95[EUR][1000 genomes]
rs7903895	0.96[EUR][1000 genomes]
rs7907187	0.96[EUR][1000 genomes]
rs7912435	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs7920488	0.98[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	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:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:26438000-26451000	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chr10:26440800-26473400	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr10:26447000-26453400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr10:26449400-26455200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr10:26450000-26451200	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr10:26450200-26452000	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr10:26450400-26452200	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr10:26450800-26451000	Enhancers	H9 Cell Line	embryonic stem cell
9	chr10:26450800-26451000	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr10:26450800-26452000	Enhancers	iPS-15b Cell Line	embryonic stem cell

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