Variant report

Variant	rs4808795
Chromosome Location	chr19:18501035-18501036
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:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:18495380..18498103-chr19:18498509..18501527,5	MCF-7	breast:
2	chr19:18439705..18442519-chr19:18499227..18501058,2	MCF-7	breast:
3	chr19:18390804..18392714-chr19:18500853..18503501,2	MCF-7	breast:
4	chr19:18302811..18308329-chr19:18497869..18501422,5	K562	blood:
5	chr19:18383403..18386564-chr19:18499646..18503057,3	K562	blood:
6	chr19:18384556..18386370-chr19:18499245..18501146,2	K562	blood:
7	chr19:18495466..18501669-chr19:18543275..18549976,8	K562	blood:
8	chr19:18413020..18415467-chr19:18499655..18501302,2	MCF-7	breast:
9	chr19:18495627..18501937-chr19:18519170..18524838,12	K562	blood:
10	chr19:18366386..18369590-chr19:18499675..18502630,3	K562	blood:
11	chr19:18450203..18453316-chr19:18500037..18503359,3	MCF-7	breast:
12	chr19:18387676..18394124-chr19:18495437..18503905,30	K562	blood:
13	chr19:18499327..18502884-chr19:18515787..18519149,4	K562	blood:
14	chr19:18494076..18504244-chr19:18508099..18514509,16	MCF-7	breast:
15	chr19:18387676..18394344-chr19:18495021..18501696,25	K562	blood:
16	chr19:18432124..18435327-chr19:18497848..18502091,4	K562	blood:
17	chr19:18448228..18453626-chr19:18495351..18501647,22	K562	blood:
18	chr19:18458959..18461482-chr19:18499425..18502890,3	K562	blood:
19	chr19:18495547..18503463-chr19:18525062..18531964,43	K562	blood:

No data

Variant related genes	Relation type
ENSG00000221167	Chromatin interaction
ENSG00000175489	Chromatin interaction
ENSG00000130517	Chromatin interaction
ENSG00000130522	Chromatin interaction
ENSG00000130513	Chromatin interaction
ENSG00000130520	Chromatin interaction
ENSG00000130511	Chromatin interaction
ENSG00000264175	Chromatin interaction
ENSG00000254858	Chromatin interaction
ENSG00000105655	Chromatin interaction
ENSG00000130518	Chromatin interaction
ENSG00000267959	Chromatin interaction

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs1059369	0.84[CEU][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12104325	0.89[ASN][1000 genomes]
rs12461382	0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1804826	0.84[CEU][hapmap];0.84[JPT][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2161106	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4808790	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4808791	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7226	0.83[CEU][hapmap];0.87[EUR][1000 genomes]
rs73011458	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8105429	0.87[EUR][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	nsv532614	chr19:18033043-18573963	Flanking Active TSS Enhancers Active TSS Genic enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	204 gene(s)	inside rSNPs	diseases
2	nsv916325	chr19:18244780-18534927	Flanking Active TSS Bivalent Enhancer Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	167 gene(s)	inside rSNPs	diseases
3	esv3323899	chr19:18343484-18620429	Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	162 gene(s)	inside rSNPs	diseases
4	nsv911274	chr19:18440942-18691942	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
5	nsv1057795	chr19:18453362-18883844	Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
6	nsv543925	chr19:18453362-18883844	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
7	nsv428018	chr19:18454891-18663981	Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
8	nsv911275	chr19:18484922-18586759	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	50 gene(s)	inside rSNPs	diseases
9	nsv2430	chr19:18496428-18514937	Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	26 gene(s)	inside rSNPs	diseases
10	nsv911276	chr19:18497141-18554972	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	47 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:60 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:18499400-18507200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr19:18499400-18508200	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr19:18499800-18501200	Strong transcription	HSMMtube	muscle
4	chr19:18499800-18501200	Genic enhancers	Monocytes-CD14+_RO01746	blood
5	chr19:18499800-18501400	Weak transcription	Rectal Mucosa Donor 29	rectum
6	chr19:18499800-18501600	Strong transcription	Lung	lung
7	chr19:18499800-18502400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr19:18499800-18502600	Genic enhancers	Primary neutrophils fromperipheralblood	blood
9	chr19:18499800-18502600	Weak transcription	NH-A	brain
10	chr19:18499800-18502800	Weak transcription	Duodenum Mucosa	Duodenum
11	chr19:18499800-18502800	Weak transcription	Gastric	stomach
12	chr19:18499800-18503400	Weak transcription	Ovary	ovary
13	chr19:18499800-18504400	Weak transcription	Adipose Nuclei	Adipose
14	chr19:18499800-18506800	Weak transcription	Colon Smooth Muscle	Colon
15	chr19:18499800-18506800	Weak transcription	Skeletal Muscle Female	skeletal muscle
16	chr19:18499800-18507200	Weak transcription	Left Ventricle	heart
17	chr19:18499800-18507200	Weak transcription	Pancreas	Pancrea
18	chr19:18499800-18507200	Weak transcription	Right Ventricle	heart
19	chr19:18499800-18507800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr19:18499800-18508200	Weak transcription	Sigmoid Colon	Sigmoid Colon
21	chr19:18499800-18508200	Weak transcription	HMEC	breast
22	chr19:18500000-18501200	Strong transcription	Liver	Liver
23	chr19:18500000-18501600	Strong transcription	Fetal Intestine Large	intestine
24	chr19:18500000-18502000	Strong transcription	Primary B cells from cord blood	blood
25	chr19:18500000-18502400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
26	chr19:18500000-18507200	Weak transcription	NHLF	lung
27	chr19:18500000-18507600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr19:18500200-18501400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr19:18500200-18501400	Genic enhancers	K562	blood
30	chr19:18500200-18502600	Genic enhancers	Primary monocytes fromperipheralblood	blood
31	chr19:18500200-18502600	Weak transcription	Stomach Mucosa	stomach
32	chr19:18500200-18502600	Weak transcription	HepG2	liver
33	chr19:18500400-18502400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
34	chr19:18500400-18502400	Strong transcription	Spleen	Spleen
35	chr19:18500400-18508000	Weak transcription	Cortex derived primary cultured neurospheres	brain
36	chr19:18500600-18501200	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr19:18500600-18501400	Strong transcription	Duodenum Smooth Muscle	Duodenum
38	chr19:18500600-18501800	ZNF genes & repeats	Fetal Intestine Small	intestine
39	chr19:18500600-18508200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr19:18500800-18501400	Genic enhancers	A549	lung
41	chr19:18500800-18501800	Strong transcription	Primary hematopoietic stem cells	blood
42	chr19:18500800-18501800	Strong transcription	Placenta	Placenta
43	chr19:18500800-18502800	Weak transcription	Primary B cells from peripheral blood	blood
44	chr19:18500800-18502800	Strong transcription	Skeletal Muscle Male	skeletal muscle
45	chr19:18500800-18503000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
46	chr19:18500800-18505400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr19:18500800-18505800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
48	chr19:18500800-18506800	Weak transcription	HSMM	muscle
49	chr19:18500800-18507200	Weak transcription	Muscle Satellite Cultured Cells	--
50	chr19:18501000-18501200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin

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