Variant report

Variant	rs9476911
Chromosome Location	chr6:15767136-15767137
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:15739404..15741557-chr6:15764680..15767519,2	K562	blood:

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10949314	0.86[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs10949315	0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12192181	0.92[AMR][1000 genomes];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12332848	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12333139	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1927575	0.86[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs2149146	0.84[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs4712256	0.85[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs4712257	0.80[AMR][1000 genomes]
rs4715997	0.85[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs6911160	0.86[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs6925866	0.86[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs6935121	0.92[AMR][1000 genomes];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs742386	0.84[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs742387	0.83[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs7739472	0.85[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs7739977	0.85[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs7756956	0.86[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs9476906	0.92[AMR][1000 genomes];0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9476912	0.86[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs9476920	0.85[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs9476921	0.94[AMR][1000 genomes];0.87[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9476922	0.85[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs9476923	0.98[ASN][1000 genomes]
rs9476934	0.80[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv428136	chr6:15595640-15781241	Enhancers Genic enhancers Weak transcription Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	esv2762581	chr6:15763793-15774802	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv518098	chr6:15764675-15771988	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 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	chr6:15759200-15770000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr6:15762200-15782000	Weak transcription	Pancreas	Pancrea
3	chr6:15764400-15768800	Weak transcription	K562	blood
4	chr6:15764800-15770200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr6:15765000-15770000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr6:15765000-15771000	Weak transcription	Gastric	stomach
7	chr6:15765600-15769200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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