Variant report

Variant	rs4808868
Chromosome Location	chr19:18988699-18988700
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2)
CpG islands
(count:0)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr19:18988598-18991468	MCF-7	breast:	n/a	n/a
2	POLR2A	chr19:18988692-18991381	Hela-S3	cervix:	n/a	n/a

No data

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:18867338..18869538-chr19:18987734..18990558,2	K562	blood:
2	chr19:18965705..18968424-chr19:18988642..18991060,2	K562	blood:
3	chr19:18985509..18988367-chr19:18988371..18990146,2	MCF-7	breast:
4	chr19:18984024..18987729-chr19:18988322..18991283,4	K562	blood:
5	chr19:18970329..18972979-chr19:18987867..18989860,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000269694	TF binding region
ENSG00000005007	Chromatin interaction

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10410987	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11673194	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.85[MEX][hapmap];0.92[TSI][hapmap];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2005695	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2018392	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4808161	0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4808163	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4808164	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4808165	0.84[CHD][hapmap];0.88[JPT][hapmap]
rs4808866	1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];1.00[TSI][hapmap];0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4808867	0.90[GIH][hapmap]
rs4808869	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4808870	1.00[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs57870078	0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7250622	0.86[MEX][hapmap]
rs7250661	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.85[MEX][hapmap];0.92[TSI][hapmap];0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7252523	0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7252796	0.81[ASN][1000 genomes]
rs7257086	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.85[MEX][hapmap];0.92[TSI][hapmap];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs73526907	0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs73526909	0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs757113	0.90[GIH][hapmap]
rs757114	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.85[MEX][hapmap];0.92[TSI][hapmap];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs886298	0.87[CEU][hapmap];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv911293	chr19:18872917-19050957	Flanking Active TSS Genic enhancers Strong transcription Active TSS Weak transcription Enhancers 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	40 gene(s)	inside rSNPs	diseases
2	nsv911294	chr19:18872917-19093619	Active TSS Weak transcription Strong transcription Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
3	nsv833777	chr19:18875936-19031076	Weak transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
4	nsv911297	chr19:18928480-19077385	Enhancers Strong transcription Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Genic enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
5	nsv911298	chr19:18928480-19093619	Weak transcription Transcr. at gene 5' and 3' Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
6	nsv911300	chr19:18944025-19093619	Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
7	nsv470132	chr19:18964442-19054720	Active TSS Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
8	nsv828473	chr19:18975130-18994875	Enhancers Strong transcription Genic enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:66 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:18979400-18989600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr19:18979600-18991800	Weak transcription	Muscle Satellite Cultured Cells	--
3	chr19:18980400-19004000	Weak transcription	Psoas Muscle	Psoas
4	chr19:18980400-19004200	Strong transcription	Cortex derived primary cultured neurospheres	brain
5	chr19:18980800-18990400	Weak transcription	Pancreas	Pancrea
6	chr19:18981000-18989200	Weak transcription	NHLF	lung
7	chr19:18981400-18998000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr19:18981800-18989400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr19:18981800-18997800	Weak transcription	Ovary	ovary
10	chr19:18981800-19005800	Weak transcription	Right Atrium	heart
11	chr19:18982000-18991400	Weak transcription	Stomach Smooth Muscle	stomach
12	chr19:18982000-19002200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr19:18982400-18995200	Strong transcription	Brain Anterior Caudate	brain
14	chr19:18982600-19000800	Weak transcription	Colon Smooth Muscle	Colon
15	chr19:18982800-18989000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr19:18983400-18998200	Strong transcription	Brain Cingulate Gyrus	brain
17	chr19:18984000-18995600	Weak transcription	Rectal Smooth Muscle	rectum
18	chr19:18984000-19004200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr19:18984600-18995000	Strong transcription	Brain Hippocampus Middle	brain
20	chr19:18984800-18995200	Strong transcription	Brain Angular Gyrus	brain
21	chr19:18984800-18995200	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
22	chr19:18985000-18989400	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr19:18985600-19004400	Weak transcription	Fetal Brain Male	brain
24	chr19:18986600-18995000	Strong transcription	Skeletal Muscle Female	skeletal muscle
25	chr19:18987200-18989200	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr19:18987200-19004200	Weak transcription	HSMMtube	muscle
27	chr19:18987400-18990000	Strong transcription	HUES64 Cell Line	embryonic stem cell
28	chr19:18987400-18991000	Weak transcription	Fetal Kidney	kidney
29	chr19:18987600-18988800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
30	chr19:18987600-18989000	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr19:18987600-18989000	Strong transcription	Pancreatic Islets	Pancreatic Islet
32	chr19:18987600-18989200	ZNF genes & repeats	Fetal Brain Female	brain
33	chr19:18987600-18989400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
34	chr19:18987600-18989600	Strong transcription	H1 Cell Line	embryonic stem cell
35	chr19:18987600-18990200	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr19:18987600-18990200	ZNF genes & repeats	Fetal Stomach	stomach
37	chr19:18987600-18990400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr19:18987800-18989800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr19:18987800-18990200	Strong transcription	iPS-15b Cell Line	embryonic stem cell
40	chr19:18988000-18989600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
41	chr19:18988000-18991000	Weak transcription	Hela-S3	cervix
42	chr19:18988000-18995200	Strong transcription	Skeletal Muscle Male	skeletal muscle
43	chr19:18988000-19005400	Weak transcription	A549	lung
44	chr19:18988200-18989000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr19:18988200-18989000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr19:18988200-18989800	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr19:18988200-18990200	Weak transcription	Fetal Lung	lung
48	chr19:18988200-18990400	Strong transcription	Brain Substantia Nigra	brain
49	chr19:18988200-18993000	Weak transcription	HUES48 Cell Line	embryonic stem cell
50	chr19:18988200-18993800	Weak transcription	Aorta	Aorta

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