Variant report

Variant	rs11527473
Chromosome Location	chr10:55261164-55261165
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 63 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10508996	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10762989	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10762990	0.86[EUR][1000 genomes]
rs10762992	0.81[EUR][1000 genomes]
rs10825030	0.85[ASN][1000 genomes]
rs10825032	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10825036	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10825037	0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10825039	0.84[ASN][1000 genomes]
rs10825040	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10825044	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10825045	0.82[ASN][1000 genomes]
rs10825046	0.82[ASN][1000 genomes]
rs10825048	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10825051	0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10825057	0.81[ASN][1000 genomes]
rs10825058	0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs10825061	0.84[EUR][1000 genomes]
rs10825062	0.81[ASN][1000 genomes]
rs11003644	0.82[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs11003648	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11003649	0.89[ASN][1000 genomes]
rs11003652	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11003660	0.82[ASN][1000 genomes]
rs11003663	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11003667	0.81[ASN][1000 genomes]
rs11527263	0.85[ASN][1000 genomes]
rs11527471	0.87[ASN][1000 genomes]
rs1157254	0.82[ASN][1000 genomes]
rs12355148	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12355167	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12358302	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12772765	0.89[ASN][1000 genomes]
rs1814085	0.82[ASN][1000 genomes]
rs28841706	0.85[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs34965206	0.84[ASN][1000 genomes]
rs351821	0.87[ASN][1000 genomes]
rs419882	0.86[ASN][1000 genomes]
rs61859857	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs61859858	0.84[ASN][1000 genomes]
rs61862612	0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7072272	0.82[ASN][1000 genomes]
rs7072928	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7080156	0.80[ASN][1000 genomes]
rs7083928	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7084959	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7097071	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7097292	0.80[ASN][1000 genomes]
rs7098611	0.83[ASN][1000 genomes]
rs996212	0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2752952	chr10:54900994-55497594	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1041908	chr10:55003164-55283251	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv540629	chr10:55003164-55283251	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv1040943	chr10:55040577-55279797	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv540630	chr10:55040577-55279797	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv1037480	chr10:55102814-55289571	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	esv2755889	chr10:55150173-55278481	Enhancers Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	nsv1048399	chr10:55151470-55313737	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	nsv1044282	chr10:55186501-55516392	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
10	nsv540631	chr10:55186501-55516392	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
11	nsv1043501	chr10:55186701-55516253	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
12	nsv540632	chr10:55186701-55516253	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
13	nsv1050323	chr10:55190079-55546575	Weak transcription ZNF genes & repeats Enhancers Active TSS Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr10:55259400-55272600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr10:55259800-55265200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr10:55259800-55268400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr10:55261000-55261600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr10:55261000-55261800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr10:55261000-55263200	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr10:55261000-55263200	Weak transcription	HUES64 Cell Line	embryonic stem cell
8	chr10:55261000-55266800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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