Variant report

Variant	rs17191127
Chromosome Location	chr15:60241774-60241775
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10519028	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12439255	0.82[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs12439270	0.90[AMR][1000 genomes];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12440475	0.86[AMR][1000 genomes];0.80[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1365115	0.81[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs1365116	0.83[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs1365117	0.83[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs1365118	0.81[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs1425929	0.97[AFR][1000 genomes];0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1425930	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs1425931	0.83[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs1582738	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs1582741	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1863394	0.86[AMR][1000 genomes];0.80[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1863395	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1991251	0.88[AFR][1000 genomes];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2059554	0.85[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs2059555	0.85[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs2059556	0.88[ASN][1000 genomes]
rs2414653	0.82[AFR][1000 genomes];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs28507628	0.81[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs4774351	0.83[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs60668087	0.80[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs62013081	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62013082	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62013083	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62013084	0.83[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs62013085	0.95[ASN][1000 genomes]
rs62013086	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62013090	0.80[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs62013091	0.82[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs62013092	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs62013093	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs62015050	0.89[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs7172033	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][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	nsv904280	chr15:60042722-60524025	Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	esv2760398	chr15:60208658-60243534	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv833028	chr15:60227565-60418112	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:60235200-60247800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr15:60241400-60242200	Enhancers	Primary hematopoietic stem cells	blood
3	chr15:60241400-60242400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr15:60241600-60242200	Enhancers	Dnd41	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links