Variant report

Variant	esv1831789
Chromosome Location	chr19:41359391-41393244
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:271)
CpG islands
(count:428)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:271 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:41370633-41370945	K562	blood:	n/a	n/a
2	ARID3A	chr19:41378197-41378436	K562	blood:	n/a	n/a
3	ATF1	chr19:41370536-41370948	K562	blood:	n/a	n/a
4	ATF1	chr19:41378237-41378485	K562	blood:	n/a	n/a
5	ATF3	chr19:41378141-41378430	K562	blood:	n/a	n/a
6	ATF3	chr19:41370620-41370877	K562	blood:	n/a	n/a
7	CBX3	chr19:41379821-41380148	K562	blood:	n/a	n/a
8	CBX3	chr19:41370123-41371107	K562	blood:	n/a	n/a
9	CBX3	chr19:41381255-41381833	K562	blood:	n/a	n/a
10	CBX3	chr19:41379769-41380227	K562	blood:	n/a	n/a
11	CCNT2	chr19:41370582-41370786	K562	blood:	n/a	n/a
12	CEBPB	chr19:41368761-41369068	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr19:41373834-41374300	A549	lung:	n/a	n/a
14	CEBPB	chr19:41378202-41378474	K562	blood:	n/a	n/a
15	CEBPB	chr19:41370543-41370910	K562	blood:	n/a	n/a
16	CEBPB	chr19:41374056-41374100	A549	lung:	n/a	n/a
17	CEBPB	chr19:41370209-41371189	K562	blood:	n/a	chr19:41370433-41370441
18	CEBPB	chr19:41368480-41368982	A549	lung:	n/a	n/a
19	CEBPB	chr19:41362024-41362201	K562	blood:	n/a	n/a
20	CEBPB	chr19:41373920-41374208	K562	blood:	n/a	n/a
21	CEBPB	chr19:41368416-41368601	K562	blood:	n/a	n/a
22	CEBPB	chr19:41378139-41378466	K562	blood:	n/a	n/a
23	CEBPB	chr19:41367289-41367476	A549	lung:	n/a	n/a
24	CEBPB	chr19:41370305-41370801	K562	blood:	n/a	chr19:41370433-41370441
25	CEBPD	chr19:41370661-41370862	K562	blood:	n/a	n/a
26	CEBPD	chr19:41392214-41392550	K562	blood:	n/a	n/a
27	CEBPD	chr19:41370295-41371143	K562	blood:	n/a	n/a
28	CTCF	chr19:41360102-41360175	K562	blood:	n/a	n/a
29	CTCF	chr19:41386284-41386617	K562	blood:	n/a	n/a
30	CTCF	chr19:41368340-41368490	HPAF	blood vessel:	n/a	n/a
31	CTCF	chr19:41368300-41368450	AG04450	lung:	n/a	n/a
32	CTCF	chr19:41368540-41368690	AoAF	blood vessel:	n/a	n/a
33	CTCF	chr19:41364158-41364220	MCF-7	breast:	n/a	n/a
34	CTCF	chr19:41381744-41381801	Spleen_OC	spleen:	n/a	n/a
35	CTCF	chr19:41368380-41368530	K562	blood:	n/a	n/a
36	CTCF	chr19:41368380-41368530	A549	lung:	n/a	n/a
37	CTCF	chr19:41368340-41368490	MCF-7	breast:	n/a	n/a
38	CTCF	chr19:41368320-41368470	HVMF	connective:	n/a	n/a
39	CTCF	chr19:41386312-41386552	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr19:41368300-41368450	MCF-7	breast:	n/a	n/a
41	CTCF	chr19:41368260-41368410	HVMF	connective:	n/a	n/a
42	CTCF	chr19:41368500-41368650	NHLF	lung:	n/a	n/a
43	CTCF	chr19:41368400-41368550	HBMEC	blood vessel:	n/a	n/a
44	CTCF	chr19:41368340-41368490	AoAF	blood vessel:	n/a	n/a
45	CTCF	chr19:41368320-41368470	AG09309	skin:	n/a	n/a
46	CTCF	chr19:41368440-41368590	HCFaa	heart:	n/a	n/a
47	CTCF	chr19:41364190-41364227	MCF-7	breast:	n/a	n/a
48	CTCF	chr19:41367560-41367710	HEK293	kidney:	n/a	n/a
49	CTCF	chr19:41381740-41381820	GM13976	blood:	n/a	n/a
50	CTCF	chr19:41368140-41368290	NHDF-neo	bronchial:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:41388232-41388282	NT2-D1	testis:	n/a
2	chr19:41388232-41388282	NT2-D1	testis:	n/a
3	chr19:41388232-41388282	NHDF-neo	bronchial:	n/a
4	chr19:41385865-41385915	HRE	kidney:	n/a
5	chr19:41388232-41388282	NH-A	brain:	n/a
6	chr19:41385865-41385915	GM06990	blood:	n/a
7	chr19:41388384-41388434	Hela-S3	cervix:	n/a
8	chr19:41385865-41385915	LNCaP	prostate:	n/a
9	chr19:41386507-41386557	AG09319	gingival:	n/a
10	chr19:41386441-41386491	HCT-116	colon:	n/a
11	chr19:41383654-41383704	Hepatocyte	liver:	n/a
12	chr19:41385865-41385915	ProgFib	skin:	n/a
13	chr19:41386507-41386557	K562	blood:	n/a
14	chr19:41388384-41388434	HEEpiC	esophagus:	n/a
15	chr19:41389684-41389734	HUVEC	blood vessel:	n/a
16	chr19:41386441-41386491	ovcar-3	ovarian:	n/a
17	chr19:41388384-41388434	IMR90	lung:	fetal
18	chr19:41388384-41388434	AG09309	skin:	n/a
19	chr19:41389684-41389734	HL-60	blood:	n/a
20	chr19:41388232-41388282	BE2_C	brain:	n/a
21	chr19:41386507-41386557	NT2-D1	testis:	n/a
22	chr19:41389684-41389734	HEK293	kidney:	embryo
23	chr19:41388384-41388434	HepG2	liver:	n/a
24	chr19:41386507-41386557	CMK	blood:	n/a
25	chr19:41389684-41389734	HCF	heart:	n/a
26	chr19:41386507-41386557	HCT-116	colon:	n/a
27	chr19:41385865-41385915	HepG2	liver:	n/a
28	chr19:41388384-41388434	GM12891	blood:	n/a
29	chr19:41385865-41385915	PrEC	prostate:	n/a
30	chr19:41385865-41385915	AoSMC	blood vessel:	n/a
31	chr19:41383654-41383704	T-47D	breast:	n/a
32	chr19:41386441-41386491	PrEC	prostate:	n/a
33	chr19:41386441-41386491	BJ	skin:	n/a
34	chr19:41383654-41383704	PANC-1	pancreas:	n/a
35	chr19:41383654-41383704	U87	brain:	n/a
36	chr19:41386507-41386557	AG09309	skin:	n/a
37	chr19:41389684-41389734	HRCEpiC	kidney:	n/a
38	chr19:41385865-41385915	Caco-2	colon:	n/a
39	chr19:41383654-41383704	LNCaP	prostate:	n/a
40	chr19:41389684-41389734	HIPEpiC	eye:	n/a
41	chr19:41388384-41388434	HRCEpiC	kidney:	n/a
42	chr19:41386441-41386491	NB4	blood:	n/a
43	chr19:41386441-41386491	LNCaP	prostate:	n/a
44	chr19:41386507-41386557	PANC-1	pancreas:	n/a
45	chr19:41386441-41386491	AG10803	skin:	n/a
46	chr19:41386441-41386491	AoSMC	blood vessel:	n/a
47	chr19:41385865-41385915	GM12878	blood:	n/a
48	chr19:41388232-41388282	A549	lung:	n/a
49	chr19:41386507-41386557	HCPEpiC	choroid plexus:	n/a
50	chr19:41383654-41383704	HCT-116	colon:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:41195484..41197379-chr19:41368669..41371255,2	K562	blood:
2	chr19:41369230..41371017-chr19:41372027..41374078,2	K562	blood:
3	chr19:41369230..41371017-chr19:41372027..41374078,2	K562	blood:

No data

Variant related genes	Relation type
CYP2G1P	TF binding region
CYP2A6	TF binding region
CYP2A7	TF binding region
CYP2G1P	CpG island
CYP2A6	CpG island
CYP2A7	CpG island
ENSG00000105245	chromatin interactions

Extended variants
information (count: 1722 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:1722 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565039434	chr19:41359398-41359399	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs532216264	chr19:41359508-41359509	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs547623862	chr19:41359541-41359542	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs565832802	chr19:41359568-41359569	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs530042413	chr19:41359615-41359616	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs114963913	chr19:41359741-41359742	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs569338202	chr19:41359742-41359743	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs200192282	chr19:41359745-41359746	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs536717230	chr19:41359761-41359762	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs534647783	chr19:41359797-41359798	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs145952075	chr19:41359884-41359885	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs375740321	chr19:41359885-41359886	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs138327641	chr19:41359893-41359894	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs372042102	chr19:41359916-41359917	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs554387075	chr19:41359921-41359922	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs183842201	chr19:41359942-41359943	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs543336528	chr19:41359962-41359963	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs3875149	chr19:41359996-41359997	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs576520588	chr19:41360058-41360059	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs537440480	chr19:41360065-41360066	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs543897659	chr19:41360077-41360078	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs565383425	chr19:41360087-41360088	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs577313552	chr19:41360114-41360115	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs373277363	chr19:41360123-41360124	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs62108999	chr19:41360188-41360189	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs11882754	chr19:41360205-41360206	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs144846156	chr19:41360226-41360227	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs374632141	chr19:41360263-41360264	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs548097776	chr19:41360278-41360279	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs562906926	chr19:41360307-41360308	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs377724348	chr19:41360311-41360312	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs530431918	chr19:41360313-41360314	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs575040003	chr19:41360316-41360317	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs570447063	chr19:41360317-41360318	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs534751836	chr19:41360355-41360356	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs76664667	chr19:41360356-41360357	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs547657467	chr19:41360361-41360362	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs566287574	chr19:41360369-41360370	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs536912355	chr19:41360370-41360371	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs535920396	chr19:41360372-41360373	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs555312091	chr19:41360382-41360383	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs576459634	chr19:41360411-41360412	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs537439747	chr19:41360461-41360462	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs559032409	chr19:41360507-41360508	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs577249588	chr19:41360526-41360527	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs541541575	chr19:41360638-41360639	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs199753395	chr19:41360681-41360682	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs189194512	chr19:41360740-41360741	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs574587414	chr19:41360807-41360808	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs541678011	chr19:41360827-41360828	Enhancers	TF binding 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
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	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	21858162	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
Ovarian cancer	22174824	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Invasive pancreatic ductal carcinoma	18765526	CNVD
Rhabdomyosarcoma	16790082	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Ovarian neoplasms	16753589	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	19029149	CNVD
Breast cancer	20409316	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Genital abnormality	22378287	CNVD
Hypospadia	22378287	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Astrocytoma	22246337	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:171 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:41356400-41362000	Enhancers	Liver	Liver
2	chr19:41358800-41360800	Weak transcription	Stomach Mucosa	stomach
3	chr19:41359600-41359800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr19:41360800-41361000	Enhancers	HSMMtube	muscle
5	chr19:41360800-41361200	Enhancers	Stomach Mucosa	stomach
6	chr19:41361000-41361600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr19:41361000-41361600	Enhancers	A549	lung
8	chr19:41361200-41361400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr19:41361400-41361800	Weak transcription	HSMMtube	muscle
10	chr19:41361400-41362400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
11	chr19:41361800-41362000	Enhancers	HSMMtube	muscle
12	chr19:41361800-41363000	Enhancers	Adipose Nuclei	Adipose
13	chr19:41362400-41368400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
14	chr19:41362800-41366000	Weak transcription	Stomach Smooth Muscle	stomach
15	chr19:41363000-41368400	Weak transcription	Adipose Nuclei	Adipose
16	chr19:41363600-41370800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr19:41365000-41365200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr19:41365200-41368200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr19:41367000-41373800	Enhancers	K562	blood
20	chr19:41367400-41370000	Enhancers	Ovary	ovary
21	chr19:41368000-41368800	Enhancers	A549	lung
22	chr19:41368200-41368400	Weak transcription	Fetal Intestine Large	intestine
23	chr19:41368200-41368800	Enhancers	HSMM	muscle
24	chr19:41368200-41368800	Enhancers	HSMMtube	muscle
25	chr19:41368200-41369000	Enhancers	Liver	Liver
26	chr19:41368200-41369200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr19:41368200-41371000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr19:41368400-41368600	Enhancers	Fetal Intestine Large	intestine
29	chr19:41368400-41368800	Enhancers	Adipose Nuclei	Adipose
30	chr19:41368400-41369000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr19:41368400-41369000	Enhancers	Hela-S3	cervix
32	chr19:41368400-41371000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
33	chr19:41368600-41369000	Enhancers	Fetal Intestine Small	intestine
34	chr19:41368600-41370800	Weak transcription	Fetal Intestine Large	intestine
35	chr19:41368800-41370600	Weak transcription	A549	lung
36	chr19:41368800-41370800	Weak transcription	Adipose Nuclei	Adipose
37	chr19:41369000-41370800	Weak transcription	Fetal Intestine Small	intestine
38	chr19:41369800-41370000	Enhancers	Primary hematopoietic stem cells short term culture	blood
39	chr19:41370000-41370800	Weak transcription	Ovary	ovary
40	chr19:41370200-41371600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr19:41370600-41371000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr19:41370600-41371200	Enhancers	A549	lung
43	chr19:41370800-41371000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr19:41370800-41371000	Enhancers	Adipose Nuclei	Adipose
45	chr19:41370800-41371200	Enhancers	Ovary	ovary
46	chr19:41370800-41371400	Enhancers	Fetal Intestine Small	intestine
47	chr19:41370800-41371600	Enhancers	Fetal Intestine Large	intestine
48	chr19:41371200-41371600	Weak transcription	A549	lung
49	chr19:41371600-41372400	Enhancers	A549	lung
50	chr19:41372400-41372800	Flanking Active TSS	A549	lung

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