Variant report

Variant	rs4808820
Chromosome Location	chr19:18681772-18681773
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:16)
CpG islands
(count:0)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:16 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	E2F4	chr19:18681638-18683070	MCF10A-Er-Src	breast:	n/a	chr19:18682942-18682954 chr19:18682479-18682488 chr19:18682621-18682630
2	POLR2A	chr19:18681493-18689919	HepG2	liver:	n/a	n/a
3	SIN3AK20	chr19:18681557-18683160	HCT-116	colon:	n/a	n/a
4	FOS	chr19:18681627-18681914	MCF10A-Er-Src	breast:	n/a	n/a
5	POLR2A	chr19:18681679-18684916	K562	blood:	n/a	n/a
6	POLR2A	chr19:18681529-18684361	PFSK-1	brain:	n/a	n/a
7	POLR2A	chr19:18681616-18683109	PANC-1	pancreas:	n/a	n/a
8	FOS	chr19:18681664-18681943	MCF10A-Er-Src	breast:	n/a	n/a
9	POLR2A	chr19:18681696-18683087	MCF-7	breast:	n/a	n/a
10	POLR2A	chr19:18681665-18684916	PFSK-1	brain:	n/a	n/a
11	FOS	chr19:18681662-18682665	MCF10A-Er-Src	breast:	n/a	chr19:18682478-18682487
12	FOS	chr19:18681630-18682661	MCF10A-Er-Src	breast:	n/a	chr19:18682478-18682487
13	POLR2A	chr19:18681589-18684803	SK-N-MC	brain:	n/a	n/a
14	POLR2A	chr19:18681647-18682021	HCT-116	colon:	n/a	n/a
15	POLR2A	chr19:18681678-18683090	MCF-7	breast:	n/a	n/a
16	POLR2A	chr19:18681642-18682012	HCT-116	colon:	n/a	n/a

No data

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:18631257..18635225-chr19:18680941..18684038,5	MCF-7	breast:
2	chr19:18629832..18635572-chr19:18680910..18686315,11	K562	blood:
3	chr19:18548448..18551673-chr19:18681148..18684161,3	K562	blood:
4	chr19:18666965..18674770-chr19:18676405..18685095,25	K562	blood:
5	chr19:18678376..18688390-chr19:18697032..18707656,34	K562	blood:
6	chr19:18651498..18655648-chr19:18680777..18683781,5	MCF-7	breast:
7	chr19:18586402..18589298-chr19:18680966..18684505,3	K562	blood:
8	chr19:18653470..18656783-chr19:18680897..18684291,6	K562	blood:
9	chr19:18681104..18684544-chr19:18745683..18749906,4	K562	blood:
10	chr19:18667097..18671007-chr19:18677068..18684435,17	K562	blood:
11	chr19:18666812..18670172-chr19:18680715..18684041,6	MCF-7	breast:
12	chr19:18628801..18634367-chr19:18680492..18684131,12	MCF-7	breast:
13	chr19:18629832..18634516-chr19:18680910..18685097,11	K562	blood:
14	chr19:18555082..18556968-chr19:18679679..18681810,2	MCF-7	breast:
15	chr19:18681312..18685117-chr19:18698049..18701447,5	MCF-7	breast:
16	chr19:18651038..18656783-chr19:18680897..18685521,14	K562	blood:

No data

Variant related genes	Relation type
ENSG00000268983	TF binding region
UBA52	TF binding region
ENSG00000006016	Chromatin interaction
ENSG00000167487	Chromatin interaction
ENSG00000105700	Chromatin interaction
ENSG00000105655	Chromatin interaction
ENSG00000268030	Chromatin interaction
ENSG00000105701	Chromatin interaction
ENSG00000105656	Chromatin interaction
ENSG00000006015	Chromatin interaction

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs11574806	1.00[CHD][hapmap]
rs34863656	1.00[CHD][hapmap]

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	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
2	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
3	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
4	nsv532615	chr19:18534867-18796031	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
5	nsv911281	chr19:18613917-18758255	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
6	nsv911282	chr19:18624964-18928480	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
7	nsv911283	chr19:18626732-18689830	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
8	nsv833776	chr19:18638028-18782264	Flanking Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Strong transcription Weak transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
9	nsv911284	chr19:18643036-18684216	Flanking Active TSS Active TSS Weak transcription Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
10	nsv911286	chr19:18652844-18811112	Active TSS Flanking Active TSS Enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:18669800-18682000	Weak transcription	Fetal Brain Male	brain
2	chr19:18669800-18682200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr19:18670600-18682000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
4	chr19:18673800-18682000	Weak transcription	Right Atrium	heart
5	chr19:18676000-18682000	Weak transcription	Fetal Kidney	kidney
6	chr19:18678000-18682000	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr19:18678400-18682000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
8	chr19:18678600-18681800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
9	chr19:18678600-18682000	Weak transcription	Psoas Muscle	Psoas
10	chr19:18679400-18681800	Weak transcription	Stomach Mucosa	stomach
11	chr19:18679600-18682000	Weak transcription	A549	lung
12	chr19:18679600-18682000	Weak transcription	NH-A	brain
13	chr19:18679600-18682000	Weak transcription	NHDF-Ad	bronchial
14	chr19:18679600-18682200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr19:18679800-18681800	Weak transcription	Primary B cells from cord blood	blood
16	chr19:18679800-18682000	Weak transcription	Brain Angular Gyrus	brain
17	chr19:18679800-18682000	Weak transcription	Fetal Lung	lung
18	chr19:18679800-18682000	Weak transcription	Hela-S3	cervix
19	chr19:18679800-18682200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr19:18679800-18682200	Weak transcription	Esophagus	oesophagus
21	chr19:18679800-18682600	Weak transcription	Small Intestine	intestine
22	chr19:18680000-18681800	Weak transcription	Rectal Mucosa Donor 31	rectum
23	chr19:18680000-18682000	Weak transcription	Brain Inferior Temporal Lobe	brain
24	chr19:18680000-18682000	Weak transcription	HSMMtube	muscle
25	chr19:18680200-18681800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
26	chr19:18680200-18682000	Weak transcription	Brain Hippocampus Middle	brain
27	chr19:18680200-18682000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
28	chr19:18680200-18682000	Weak transcription	Brain Substantia Nigra	brain
29	chr19:18680200-18682000	Weak transcription	Colon Smooth Muscle	Colon
30	chr19:18680200-18682200	Weak transcription	Ovary	ovary
31	chr19:18680400-18681800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr19:18680400-18681800	Weak transcription	Primary T helper cells PMA-I stimulated	--
33	chr19:18680400-18681800	Weak transcription	Primary T helper cells fromperipheralblood	blood
34	chr19:18680400-18681800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
35	chr19:18680400-18681800	Weak transcription	Adipose Nuclei	Adipose
36	chr19:18680400-18681800	Weak transcription	Colonic Mucosa	Colon
37	chr19:18680400-18681800	Weak transcription	Duodenum Mucosa	Duodenum
38	chr19:18680400-18681800	Weak transcription	Lung	lung
39	chr19:18680400-18681800	Weak transcription	Right Ventricle	heart
40	chr19:18680400-18681800	Weak transcription	Stomach Smooth Muscle	stomach
41	chr19:18680400-18681800	Weak transcription	HepG2	liver
42	chr19:18680400-18681800	Weak transcription	HMEC	breast
43	chr19:18680400-18682000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr19:18680400-18682000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
45	chr19:18680400-18682000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr19:18680400-18682000	Weak transcription	Brain Cingulate Gyrus	brain
47	chr19:18680400-18682000	Weak transcription	Left Ventricle	heart
48	chr19:18680400-18682000	Weak transcription	Skeletal Muscle Male	skeletal muscle
49	chr19:18680400-18682000	Weak transcription	Skeletal Muscle Female	skeletal muscle
50	chr19:18680400-18682000	Weak transcription	HUVEC	blood vessel

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