Variant report

Variant	rs4775025
Chromosome Location	chr15:58513997-58513998
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:57851915..57852687-chr15:58513623..58514467,2	K562	blood:
2	chr15:58504304..58505276-chr15:58513365..58514203,2	MCF-7	breast:
3	chr15:58477664..58478358-chr15:58513555..58514482,3	MCF-7	breast:
4	chr15:58513464..58515183-chr15:58519032..58521453,2	K562	blood:
5	chr15:58407482..58408061-chr15:58513659..58514466,2	MCF-7	breast:
6	chr15:58504905..58505726-chr15:58513648..58514433,4	MCF-7	breast:
7	chr15:58369177..58370015-chr15:58513534..58514314,2	K562	blood:
8	chr15:58261244..58261767-chr15:58513997..58514512,2	K562	blood:
9	chr15:58474504..58475220-chr15:58513550..58514293,3	K562	blood:
10	chr15:58504835..58508448-chr15:58511770..58515596,3	K562	blood:
11	chr15:57853056..57853844-chr15:58513573..58514501,2	K562	blood:

No data

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

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10518967	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11631950	0.80[ASN][1000 genomes]
rs12439244	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12439277	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12439347	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12442501	0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1618701	0.89[ASN][1000 genomes]
rs1663253	0.86[ASN][1000 genomes]
rs1663254	0.88[ASN][1000 genomes]
rs1663255	0.93[ASN][1000 genomes]
rs2017566	0.86[ASN][1000 genomes]
rs2414551	0.89[ASN][1000 genomes]
rs2414552	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3742958	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4350519	0.85[ASN][1000 genomes]
rs4375604	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4775023	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4775026	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58238893	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7162995	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7173910	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7180071	0.88[ASN][1000 genomes]
rs8032239	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9788656	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1047246	chr15:58375607-58707158	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv833024	chr15:58447459-58621963	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv1050473	chr15:58479888-58562270	Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv904264	chr15:58505122-58588510	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:58502800-58516200	Weak transcription	NHEK	skin
2	chr15:58505800-58516200	Weak transcription	Right Atrium	heart
3	chr15:58506400-58515000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr15:58506400-58515200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr15:58506600-58520200	Weak transcription	Liver	Liver
6	chr15:58512600-58516200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr15:58513600-58517000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr15:58513600-58517200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr15:58513800-58514000	Enhancers	H9 Cell Line	embryonic stem cell
10	chr15:58513800-58514000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr15:58513800-58514000	Enhancers	Spleen	Spleen

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