Variant report

Variant	esv3318822
Chromosome Location	chr19:51105140-51110238
allele	n/a
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:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:51103969..51106972-chr19:51302826..51304990,3	K562	blood:
2	chr19:51059824..51061541-chr19:51102539..51105453,2	K562	blood:
3	chr19:51105210..51106764-chr19:51296992..51298664,2	K562	blood:
4	chr19:51103570..51107800-chr19:51108221..51112163,4	K562	blood:
5	chr19:51109906..51112856-chr19:51294280..51296293,2	K562	blood:
6	chr19:51109418..51112978-chr19:51159521..51162574,6	K562	blood:
7	chr19:51103150..51105218-chr19:51609858..51612027,2	MCF-7	breast:
8	chr19:51104377..51107028-chr19:51160247..51163970,4	K562	blood:
9	chr19:51109418..51112998-chr19:51159027..51162201,6	K562	blood:
10	chr19:51102852..51106363-chr19:51160109..51162929,6	K562	blood:
11	chr19:51103570..51107800-chr19:51108221..51112163,4	K562	blood:
12	chr19:51105143..51107316-chr19:51152690..51155316,2	K562	blood:
13	chr19:51108915..51112953-chr19:51162682..51166555,5	K562	blood:
14	chr19:51110056..51112953-chr19:51162682..51165400,3	K562	blood:

No data

Variant related genes	Relation type
ENSG00000161681	chromatin interactions
ENSG00000268231	chromatin interactions
ENSG00000142544	chromatin interactions
ENSG00000235034	chromatin interactions

Extended variants
information (count: 254 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:254 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs112634058	chr19:51105169-51105170	Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs551338148	chr19:51105183-51105184	Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs148217386	chr19:51105193-51105194	Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs141175056	chr19:51105196-51105197	Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs150291261	chr19:51105205-51105206	Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs575635234	chr19:51105261-51105262	Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs568164404	chr19:51105310-51105311	Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs535595044	chr19:51105395-51105396	Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs553799587	chr19:51105501-51105502	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs191207959	chr19:51105502-51105503	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs368428526	chr19:51105503-51105504	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs539467507	chr19:51105529-51105530	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs73590650	chr19:51105537-51105538	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs576247593	chr19:51105583-51105584	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs376349684	chr19:51105662-51105663	Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs543150720	chr19:51105769-51105770	Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs138157776	chr19:51105770-51105771	Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs574165363	chr19:51105818-51105819	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs10413426	chr19:51105859-51105860	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs559644831	chr19:51105872-51105873	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs546265573	chr19:51105918-51105919	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs142631393	chr19:51105925-51105926	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs181556709	chr19:51105926-51105927	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs545040765	chr19:51106007-51106008	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs560967900	chr19:51106012-51106013	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs563338228	chr19:51106013-51106014	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs8107374	chr19:51106019-51106020	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs549216877	chr19:51106055-51106056	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs62112489	chr19:51106089-51106090	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs567716416	chr19:51106093-51106094	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs558547437	chr19:51106116-51106117	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs8106843	chr19:51106148-51106149	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs35031768	chr19:51106157-51106158	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs371947695	chr19:51106184-51106185	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs186573140	chr19:51106201-51106202	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs191891504	chr19:51106203-51106204	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs376563343	chr19:51106207-51106208	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs141297950	chr19:51106210-51106211	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs569556305	chr19:51106247-51106248	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs537012708	chr19:51106271-51106272	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs369205227	chr19:51106293-51106294	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs376159064	chr19:51106403-51106404	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs6509489	chr19:51106421-51106422	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
44	rs541294946	chr19:51106453-51106454	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs553139460	chr19:51106456-51106457	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs371807632	chr19:51106468-51106469	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs577963985	chr19:51106478-51106479	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs374644816	chr19:51106487-51106488	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs367952093	chr19:51106489-51106490	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs139464247	chr19:51106490-51106491	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Ovarian cancer	21720365	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Ductal carcinoma	22052326	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	17603634	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
renal disease	20603712	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Acute myeloid leukemia	20729466	CNVD
Hepatocellular carcinoma	16750200	CNVD
Colorectal cancer	20459617	CNVD
Ovarian cancer	22174824	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Wilms tumour	21544195	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Congenital anomalies of the kidney and urinary tract	18852474	CNVD
Glioblastoma multiforme	17002787	CNVD
Cervical cancer	21062161	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Basal cell lymphoma	19029149	CNVD
Breast cancer	20409316	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Cancer	17160897	CNVD
Prostate cancer	16573809	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Adrenocortical carcinoma	18281524	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:35 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:51103000-51105600	Enhancers	HUVEC	blood vessel
2	chr19:51104400-51105600	Flanking Active TSS	K562	blood
3	chr19:51105600-51105800	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr19:51105600-51106800	Enhancers	K562	blood
5	chr19:51106800-51109000	Weak transcription	K562	blood
6	chr19:51107800-51108000	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
7	chr19:51107800-51109800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr19:51109000-51109200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
9	chr19:51109000-51109200	Enhancers	Brain Inferior Temporal Lobe	brain
10	chr19:51109000-51109400	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
11	chr19:51109000-51109400	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
12	chr19:51109000-51109400	Enhancers	Brain Angular Gyrus	brain
13	chr19:51109000-51109400	Bivalent/Poised TSS	A549	lung
14	chr19:51109000-51109400	Flanking Active TSS	K562	blood
15	chr19:51109000-51109800	Active TSS	Brain Substantia Nigra	brain
16	chr19:51109000-51110800	Active TSS	Brain Anterior Caudate	brain
17	chr19:51109000-51110800	Enhancers	Brain Hippocampus Middle	brain
18	chr19:51109200-51109400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
19	chr19:51109200-51109400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr19:51109200-51109400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr19:51109200-51109400	Flanking Active TSS	Brain Cingulate Gyrus	brain
22	chr19:51109200-51109400	Bivalent Enhancer	Fetal Muscle Leg	muscle
23	chr19:51109200-51109400	Bivalent Enhancer	Placenta	Placenta
24	chr19:51109200-51109800	Active TSS	Brain Inferior Temporal Lobe	brain
25	chr19:51109400-51109600	Bivalent Enhancer	Fetal Brain Male	brain
26	chr19:51109400-51109800	Enhancers	Brain Cingulate Gyrus	brain
27	chr19:51109400-51110200	Enhancers	K562	blood
28	chr19:51109400-51110800	Weak transcription	Brain Angular Gyrus	brain
29	chr19:51109800-51110000	Bivalent/Poised TSS	Primary T cells from cord blood	blood
30	chr19:51109800-51110000	Active TSS	Brain Cingulate Gyrus	brain
31	chr19:51109800-51110600	Weak transcription	Brain Inferior Temporal Lobe	brain
32	chr19:51109800-51110600	Weak transcription	Brain Substantia Nigra	brain
33	chr19:51109800-51111000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr19:51110000-51110800	Weak transcription	Brain Cingulate Gyrus	brain
35	chr19:51110200-51110600	Weak transcription	K562	blood

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