Variant report

Variant	rs604453
Chromosome Location	chr18:11948532-11948533
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	chr18:11947643..11949972-chr18:11979673..11983782,3	MCF-7	breast:
2	chr18:11908313..11910629-chr18:11947415..11948984,2	K562	blood:
3	chr18:11908313..11910422-chr18:11947484..11949382,3	K562	blood:
4	chr18:11945871..11949775-chr18:11972448..11976477,3	K562	blood:
5	chr18:11944456..11952400-chr18:11978684..11982486,15	K562	blood:
6	chr18:11938000..11939656-chr18:11946087..11948724,2	K562	blood:
7	chr18:11945775..11953098-chr18:11977697..11982837,16	K562	blood:
8	chr18:11927997..11930119-chr18:11947025..11949213,2	K562	blood:
9	chr18:11907115..11909589-chr18:11947697..11950690,2	MCF-7	breast:
10	chr18:11946068..11950381-chr18:11979395..11982010,5	MCF-7	breast:
11	chr18:11947580..11949116-chr18:11949691..11952333,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000154889	Chromatin interaction
ENSG00000267661	Chromatin interaction
ENSG00000273141	Chromatin interaction
ENSG00000141401	Chromatin interaction

Extended variants
information (count: 30 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs1811452	0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs34478333	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs34803006	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs35932750	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs591880	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs604427	0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs622863	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs629550	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs648676	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs649039	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs649459	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs662981	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs677254	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs677359	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs679158	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs694635	0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7226885	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7227036	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9952563	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9962395	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3362008	chr18:11647654-11959830	Active TSS Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
2	nsv1055453	chr18:11776790-12110135	Weak transcription Active TSS Enhancers Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
3	nsv543654	chr18:11776790-12110135	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
4	esv2758470	chr18:11897023-12076102	Strong transcription Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
5	esv2758713	chr18:11897023-12076102	Flanking Active TSS Active TSS Enhancers Genic enhancers Weak transcription Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
6	nsv909384	chr18:11907374-12101109	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	42 gene(s)	inside rSNPs	diseases
7	nsv1063339	chr18:11909588-11979264	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
8	nsv576495	chr18:11917410-11986557	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
9	nsv909385	chr18:11938102-11986557	Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	20 gene(s)	inside rSNPs	diseases
10	nsv909386	chr18:11938102-12095950	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs604453	RP11-820I16.1	cis	Esophagus Muscularis	GTEx
rs604453	RP11-820I16.1	cis	Thyroid	GTEx

Chromatin state (count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:11947800-11948600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr18:11947800-11948800	Weak transcription	Fetal Lung	lung
3	chr18:11947800-11948800	Weak transcription	HepG2	liver
4	chr18:11947800-11949000	Enhancers	HSMMtube	muscle
5	chr18:11947800-11949200	Enhancers	NHDF-Ad	bronchial
6	chr18:11947800-11952400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr18:11947800-11954600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr18:11947800-11955000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr18:11948000-11948600	Enhancers	Fetal Muscle Leg	muscle
10	chr18:11948000-11948800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr18:11948000-11948800	Weak transcription	NHLF	lung
12	chr18:11948000-11949200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr18:11948000-11949200	Enhancers	Placenta	Placenta
14	chr18:11948000-11950600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr18:11948000-11951600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr18:11948000-11954400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr18:11948200-11948600	Weak transcription	HSMM	muscle
18	chr18:11948200-11948600	Weak transcription	NH-A	brain
19	chr18:11948200-11948800	Weak transcription	H1 Cell Line	embryonic stem cell
20	chr18:11948200-11948800	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr18:11948200-11948800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
22	chr18:11948200-11948800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
23	chr18:11948200-11948800	Weak transcription	Colon Smooth Muscle	Colon
24	chr18:11948200-11948800	Weak transcription	Lung	lung
25	chr18:11948200-11948800	Weak transcription	Ovary	ovary
26	chr18:11948200-11948800	Enhancers	Osteobl	bone
27	chr18:11948200-11949000	Weak transcription	HUES64 Cell Line	embryonic stem cell
28	chr18:11948200-11949000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr18:11948200-11949000	Enhancers	Fetal Stomach	stomach
30	chr18:11948200-11949200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr18:11948200-11949400	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr18:11948200-11949400	Enhancers	HUES6 Cell Line	embryonic stem cell
33	chr18:11948200-11949400	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr18:11948200-11949400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr18:11948200-11949400	Enhancers	Pancreas	Pancrea
36	chr18:11948200-11949800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr18:11948200-11950000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr18:11948200-11950000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr18:11948200-11950000	Enhancers	Muscle Satellite Cultured Cells	--
40	chr18:11948200-11951400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr18:11948200-11951600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr18:11948200-11951600	Weak transcription	Cortex derived primary cultured neurospheres	brain
43	chr18:11948200-11951600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr18:11948200-11951600	Enhancers	K562	blood
45	chr18:11948200-11951800	Weak transcription	Esophagus	oesophagus
46	chr18:11948200-11952200	Weak transcription	NHEK	skin
47	chr18:11948400-11948600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
48	chr18:11948400-11948600	Active TSS	Hela-S3	cervix
49	chr18:11948400-11948800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr18:11948400-11948800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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