Variant report

Variant	rs61383190
Chromosome Location	chr18:11984574-11984575
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr18:11951098..11953868-chr18:11983215..11985135,2	K562	blood:
2	chr18:11979366..11983605-chr18:11984399..11987435,4	MCF-7	breast:
3	chr18:11906857..11909388-chr18:11984502..11986604,2	K562	blood:
4	chr18:11977841..11980802-chr18:11983345..11984923,2	MCF-7	breast:

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

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs16976887	0.90[ASN][1000 genomes]
rs28475846	0.90[ASN][1000 genomes]
rs28499558	0.90[ASN][1000 genomes]
rs28509217	0.90[ASN][1000 genomes]
rs28548932	0.90[ASN][1000 genomes]
rs4239304	0.90[ASN][1000 genomes]
rs56364728	0.90[ASN][1000 genomes]
rs57967783	0.89[ASN][1000 genomes]
rs58556096	0.88[ASN][1000 genomes]
rs59796048	0.90[ASN][1000 genomes]
rs59889312	0.90[ASN][1000 genomes]
rs604420	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6505700	0.90[ASN][1000 genomes]
rs6505701	0.90[ASN][1000 genomes]
rs653073	0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs663591	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67932171	0.90[ASN][1000 genomes]
rs7230346	0.90[ASN][1000 genomes]
rs72871698	0.90[ASN][1000 genomes]
rs72871700	0.90[ASN][1000 genomes]
rs72871702	0.90[ASN][1000 genomes]
rs72873509	0.90[ASN][1000 genomes]
rs72873510	0.90[ASN][1000 genomes]
rs7407928	0.90[ASN][1000 genomes]
rs7506045	0.90[ASN][1000 genomes]
rs8095694	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9973177	0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	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
4	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
5	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
6	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
7	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
8	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
9	nsv909387	chr18:11953187-11986557	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	18 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:85 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:11982400-11987600	Weak transcription	Fetal Heart	heart
2	chr18:11982400-11988400	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr18:11982400-12005000	Weak transcription	Aorta	Aorta
4	chr18:11982600-11985600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr18:11982600-11985800	Weak transcription	Right Atrium	heart
6	chr18:11982600-11986800	Weak transcription	Brain Germinal Matrix	brain
7	chr18:11982600-11987400	Weak transcription	Rectal Smooth Muscle	rectum
8	chr18:11982600-11987800	Weak transcription	NHLF	lung
9	chr18:11982600-11995600	Weak transcription	Primary T cells from cord blood	blood
10	chr18:11982600-11995800	Weak transcription	Thymus	Thymus
11	chr18:11982600-12028600	Weak transcription	Small Intestine	intestine
12	chr18:11982800-11984600	Flanking Active TSS	Hela-S3	cervix
13	chr18:11983000-11984600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr18:11983200-11984600	Enhancers	Stomach Mucosa	stomach
15	chr18:11983200-11984800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr18:11983400-11984600	Enhancers	Rectal Mucosa Donor 29	rectum
17	chr18:11983400-11985600	Weak transcription	K562	blood
18	chr18:11983400-11985800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
19	chr18:11983400-11986200	Weak transcription	Ovary	ovary
20	chr18:11983400-11987400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr18:11983400-11989000	Weak transcription	Duodenum Smooth Muscle	Duodenum
22	chr18:11983400-11989200	Enhancers	Primary monocytes fromperipheralblood	blood
23	chr18:11983400-11989600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr18:11983400-11994000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr18:11983600-11989400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr18:11983800-11985600	Weak transcription	Fetal Intestine Small	intestine
27	chr18:11983800-11986600	Weak transcription	Primary hematopoietic stem cells	blood
28	chr18:11984000-11985600	Weak transcription	Right Ventricle	heart
29	chr18:11984000-11986800	Weak transcription	Stomach Smooth Muscle	stomach
30	chr18:11984000-11989000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr18:11984200-11984600	Genic enhancers	HUES48 Cell Line	embryonic stem cell
32	chr18:11984200-11984600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr18:11984200-11984600	Enhancers	HepG2	liver
34	chr18:11984200-11984600	Enhancers	HSMMtube	muscle
35	chr18:11984200-11984800	Strong transcription	Fetal Stomach	stomach
36	chr18:11984200-11985600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
37	chr18:11984200-11985800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr18:11984200-11985800	Weak transcription	Liver	Liver
39	chr18:11984200-11987000	Weak transcription	Adipose Nuclei	Adipose
40	chr18:11984200-11987400	Weak transcription	Fetal Lung	lung
41	chr18:11984200-11988200	Weak transcription	Rectal Mucosa Donor 31	rectum
42	chr18:11984200-11988400	Weak transcription	Fetal Intestine Large	intestine
43	chr18:11984200-11989800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr18:11984200-11993600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr18:11984200-11994600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr18:11984400-11984600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr18:11984400-11984600	Active TSS	Pancreas	Pancrea
48	chr18:11984400-11984800	Enhancers	Skeletal Muscle Female	skeletal muscle
49	chr18:11984400-11985200	Weak transcription	Cortex derived primary cultured neurospheres	brain
50	chr18:11984400-11985400	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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