Variant report

Variant	rs11766318
Chromosome Location	chr7:13819065-13819066
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10950488	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11761278	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11762620	0.87[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11768005	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11769506	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12670695	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13224814	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs17167514	0.87[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2108153	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs34012999	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs34492537	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs35297959	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs35454895	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs35505150	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs36041244	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs36198434	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs36200990	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs59760170	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs62452166	0.88[ASN][1000 genomes]
rs62455263	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs62455264	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs62455265	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62455267	0.84[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6974368	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6974390	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6974719	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7795241	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs9770328	0.91[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs9771428	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830909	chr7:13692329-13868294	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv887695	chr7:13704951-13819968	Active TSS ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv1019873	chr7:13707148-14133367	Bivalent Enhancer Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv1034411	chr7:13743365-13826756	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
5	nsv433032	chr7:13792450-13911001	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv887696	chr7:13801825-13857235	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:13808400-13820200	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr7:13813200-13824200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr7:13818200-13819600	Enhancers	Muscle Satellite Cultured Cells	--
4	chr7:13818200-13819800	Enhancers	Osteobl	bone
5	chr7:13818400-13819600	Enhancers	NHEK	skin
6	chr7:13818600-13819200	Enhancers	HSMM	muscle
7	chr7:13818600-13819400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr7:13818600-13819600	Enhancers	HMEC	breast
9	chr7:13818600-13819600	Enhancers	NH-A	brain
10	chr7:13818800-13819200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr7:13818800-13819200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr7:13818800-13824600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr7:13819000-13819600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
14	chr7:13819000-13819600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr7:13819000-13820600	Enhancers	Pancreatic Islets	Pancreatic Islet

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