Variant report

Variant	rs11634466
Chromosome Location	chr15:50124635-50124636
allele	A/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	chr15:50124508..50125493-chr15:50343834..50344700,3	MCF-7	breast:
2	chr15:49930555..49931785-chr15:50124192..50125413,7	MCF-7	breast:
3	chr15:49906396..49908796-chr15:50121690..50125085,3	MCF-7	breast:
4	chr15:49813617..49814647-chr15:50124460..50125524,4	MCF-7	breast:
5	chr15:49911896..49914625-chr15:50123253..50125485,3	MCF-7	breast:
6	chr15:49912462..49913074-chr15:50124499..50125268,2	MCF-7	breast:
7	chr15:50124105..50124982-chr5:57921872..57922373,2	MCF-7	breast:
8	chr15:49898526..49899536-chr15:50124520..50125405,5	MCF-7	breast:
9	chr15:49914595..49915377-chr15:50124565..50125477,5	MCF-7	breast:
10	chr15:50124501..50125449-chr15:50167403..50168098,3	MCF-7	breast:
11	chr15:49914376..49915416-chr15:50124445..50125402,4	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000166262	Chromatin interaction
ENSG00000104047	Chromatin interaction

Extended variants
information (count: 67 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:61)

rs_ID	r²[population]
rs11070724	0.98[ASN][1000 genomes]
rs11070727	0.90[AMR][1000 genomes];0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11070728	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11070729	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11070731	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11634432	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11634538	0.98[ASN][1000 genomes]
rs11635995	0.97[ASN][1000 genomes]
rs11855340	0.97[ASN][1000 genomes]
rs11858914	0.90[ASN][1000 genomes]
rs12438404	0.94[ASN][1000 genomes]
rs12440711	0.96[ASN][1000 genomes]
rs12442186	0.96[ASN][1000 genomes]
rs12442880	0.96[ASN][1000 genomes]
rs12904515	0.95[ASN][1000 genomes]
rs12909601	0.96[ASN][1000 genomes]
rs12911756	0.98[ASN][1000 genomes]
rs12912869	0.98[ASN][1000 genomes]
rs1395882	0.95[ASN][1000 genomes]
rs1395883	0.95[ASN][1000 genomes]
rs1395885	0.95[ASN][1000 genomes]
rs1395886	0.94[ASN][1000 genomes]
rs1507584	0.95[ASN][1000 genomes]
rs1507585	0.95[ASN][1000 genomes]
rs1507586	0.95[ASN][1000 genomes]
rs1588122	0.95[ASN][1000 genomes]
rs1828041	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1828042	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1848282	0.95[ASN][1000 genomes]
rs1848283	0.95[ASN][1000 genomes]
rs1848284	0.95[ASN][1000 genomes]
rs2102383	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2413967	0.95[ASN][1000 genomes]
rs2413968	0.98[ASN][1000 genomes]
rs2413969	0.98[ASN][1000 genomes]
rs2413970	0.95[ASN][1000 genomes]
rs2413971	0.91[ASN][1000 genomes]
rs2452535	0.95[ASN][1000 genomes]
rs2452537	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2452538	0.95[ASN][1000 genomes]
rs2456840	0.95[ASN][1000 genomes]
rs2456841	0.95[ASN][1000 genomes]
rs2456842	0.93[ASN][1000 genomes]
rs2660966	0.95[ASN][1000 genomes]
rs2899438	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs34614239	0.95[ASN][1000 genomes]
rs34696884	0.86[ASN][1000 genomes]
rs35816674	0.96[ASN][1000 genomes]
rs35861473	0.96[ASN][1000 genomes]
rs4404008	0.97[ASN][1000 genomes]
rs4526969	0.96[ASN][1000 genomes]
rs4551980	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4774546	0.95[ASN][1000 genomes]
rs4774547	0.88[ASN][1000 genomes]
rs4774548	0.85[ASN][1000 genomes]
rs71124308	0.87[ASN][1000 genomes]
rs7182178	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7182911	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8039234	0.97[ASN][1000 genomes]
rs873107	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs937169	0.92[ASN][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	nsv1044277	chr15:49921547-50702386	Enhancers Active TSS Weak transcription Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	107 gene(s)	inside rSNPs	diseases
2	nsv542380	chr15:49921547-50702386	Enhancers Strong transcription Weak transcription Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	107 gene(s)	inside rSNPs	diseases
3	nsv1047047	chr15:50070224-50125096	Enhancers Strong transcription Weak transcription Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv1042311	chr15:50083175-50125096	Enhancers Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	esv2761888	chr15:50083187-50125108	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv833003	chr15:50100372-50273309	ZNF genes & repeats Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:50120200-50126000	Weak transcription	Psoas Muscle	Psoas
2	chr15:50122400-50124800	Enhancers	Adipose Nuclei	Adipose
3	chr15:50122400-50125000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr15:50122400-50125200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr15:50122600-50125200	Enhancers	NHDF-Ad	bronchial
6	chr15:50122600-50125200	Enhancers	Osteobl	bone
7	chr15:50122800-50125200	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr15:50122800-50125200	Enhancers	NHLF	lung
9	chr15:50123400-50125000	Enhancers	NH-A	brain
10	chr15:50123400-50125200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr15:50123400-50125200	Enhancers	A549	lung
12	chr15:50123400-50125200	Enhancers	Hela-S3	cervix
13	chr15:50123600-50124800	Enhancers	Muscle Satellite Cultured Cells	--
14	chr15:50123600-50124800	Enhancers	HSMM	muscle
15	chr15:50123600-50125200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr15:50123800-50124800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr15:50123800-50124800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr15:50124000-50125000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr15:50124000-50125000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr15:50124000-50130200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
21	chr15:50124400-50130200	Weak transcription	Primary neutrophils fromperipheralblood	blood
22	chr15:50124600-50124800	Enhancers	Rectal Mucosa Donor 31	rectum

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