Variant report

Variant	nsv596897
Chromosome Location	chr5:1924628-1934490
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr5:1933301-1933328	K562	blood:	n/a	n/a
2	BACH1	chr5:1931242-1932154	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr5:1934036-1934438	K562	blood:	n/a	n/a
4	BHLHE40	chr5:1927394-1927444	A549	lung:	n/a	n/a
5	CBX3	chr5:1934067-1934448	K562	blood:	n/a	n/a
6	CEBPB	chr5:1928552-1928667	HepG2	liver:	n/a	chr5:1928599-1928610 chr5:1928598-1928611
7	CEBPB	chr5:1930222-1930375	H1-hESC	embryonic stem cell:	n/a	n/a
8	CHD1	chr5:1931546-1931606	H1-hESC	embryonic stem cell:	n/a	n/a
9	CHD2	chr5:1931533-1931640	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTBP2	chr5:1931111-1932029	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTCF	chr5:1930421-1930566	GM19239	blood:	n/a	n/a
12	CTCF	chr5:1929709-1930029	NHEK	skin:	n/a	n/a
13	CTCF	chr5:1929185-1930322	GM19239	blood:	n/a	n/a
14	CTCF	chr5:1934340-1934490	HMEC	breast:	n/a	n/a
15	CTCF	chr5:1930413-1930418	GM19239	blood:	n/a	n/a
16	CTCF	chr5:1934320-1934470	HepG2	liver:	n/a	n/a
17	CTCF	chr5:1934280-1934430	HCT-116	colon:	n/a	n/a
18	CTCF	chr5:1934320-1934470	GM12871	blood:	n/a	n/a
19	CTCF	chr5:1930404-1930410	GM19239	blood:	n/a	n/a
20	CTCF	chr5:1934380-1934530	K562	blood:	n/a	n/a
21	CTCF	chr5:1934324-1934533	K562	blood:	n/a	n/a
22	CTCF	chr5:1931160-1931310	NHEK	skin:	n/a	n/a
23	CTCF	chr5:1929633-1929712	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr5:1933360-1933510	GM12868	blood:	n/a	n/a
25	CTCF	chr5:1934110-1934624	K562	blood:	n/a	n/a
26	CTCF	chr5:1934361-1934475	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr5:1929301-1929371	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr5:1934349-1934497	K562	blood:	n/a	n/a
29	CTCF	chr5:1929366-1929400	NHEK	skin:	n/a	n/a
30	CTCF	chr5:1934256-1934519	K562	blood:	n/a	n/a
31	CTCF	chr5:1929718-1929720	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr5:1929776-1929814	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr5:1934300-1934570	HCT-116	colon:	n/a	n/a
34	CTCF	chr5:1934294-1934513	K562	blood:	n/a	n/a
35	CTCF	chr5:1934340-1934490	K562	blood:	n/a	n/a
36	CTCF	chr5:1930169-1930265	NHEK	skin:	n/a	n/a
37	CTCF	chr5:1934300-1934450	WERI-Rb-1	eye:	n/a	n/a
38	E2F4	chr5:1931726-1931995	MCF10A-Er-Src	breast:	n/a	n/a
39	E2F6	chr5:1933879-1934485	K562	blood:	n/a	n/a
40	EGR1	chr5:1931137-1931583	H1-hESC	embryonic stem cell:	n/a	chr5:1931259-1931268 chr5:1931258-1931271 chr5:1931258-1931271
41	EGR1	chr5:1934038-1934286	K562	blood:	n/a	chr5:1934159-1934168
42	EP300	chr5:1933964-1934389	K562	blood:	n/a	n/a
43	FOS	chr5:1933517-1933860	MCF10A-Er-Src	breast:	n/a	chr5:1933699-1933706 chr5:1933699-1933707 chr5:1933698-1933708 chr5:1933699-1933707 chr5:1933698-1933708 chr5:1933698-1933708 chr5:1933697-1933709 chr5:1933698-1933708
44	FOS	chr5:1933352-1933871	MCF10A-Er-Src	breast:	n/a	chr5:1933699-1933706 chr5:1933699-1933707 chr5:1933698-1933708 chr5:1933699-1933707 chr5:1933698-1933708 chr5:1933698-1933708 chr5:1933697-1933709 chr5:1933698-1933708
45	FOS	chr5:1933590-1933874	MCF10A-Er-Src	breast:	n/a	chr5:1933699-1933706 chr5:1933699-1933707 chr5:1933698-1933708 chr5:1933699-1933707 chr5:1933698-1933708 chr5:1933698-1933708 chr5:1933697-1933709 chr5:1933698-1933708
46	FOS	chr5:1933519-1933861	MCF10A-Er-Src	breast:	n/a	chr5:1933699-1933706 chr5:1933699-1933707 chr5:1933698-1933708 chr5:1933699-1933707 chr5:1933698-1933708 chr5:1933698-1933708 chr5:1933697-1933709 chr5:1933698-1933708
47	FOSL1	chr5:1933406-1934456	HCT-116	colon:	n/a	chr5:1933699-1933706 chr5:1934197-1934206 chr5:1933699-1933707 chr5:1933698-1933708 chr5:1933699-1933707 chr5:1933698-1933708 chr5:1933698-1933708 chr5:1933697-1933709 chr5:1933698-1933708
48	FOSL1	chr5:1933341-1934506	HCT-116	colon:	n/a	chr5:1933699-1933706 chr5:1934197-1934206 chr5:1933699-1933707 chr5:1933698-1933708 chr5:1933699-1933707 chr5:1933698-1933708 chr5:1933698-1933708 chr5:1933697-1933709 chr5:1933698-1933708
49	GABPA	chr5:1931734-1932076	H1-hESC	embryonic stem cell:	n/a	n/a
50	GABPA	chr5:1931141-1931648	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:1931781-1931831	ECC-1	luminal epithelium:	n/a
2	chr5:1931781-1931831	ECC-1	luminal epithelium:	n/a
3	chr5:1931544-1931594	LNCaP	prostate:	n/a
4	chr5:1934165-1934215	HepG2	liver:	n/a
5	chr5:1927225-1927275	AG10803	skin:	n/a
6	chr5:1930801-1930851	MCF-7	breast:	n/a
7	chr5:1931620-1931670	PFSK-1	brain:	n/a
8	chr5:1931544-1931594	HEEpiC	esophagus:	n/a
9	chr5:1931376-1931426	H1-hESC	embryonic stem cell:	embryo
10	chr5:1934165-1934215	NB4	blood:	n/a
11	chr5:1931376-1931426	HEEpiC	esophagus:	n/a
12	chr5:1931544-1931594	GM12878	blood:	n/a
13	chr5:1931251-1931301	AG09309	skin:	n/a
14	chr5:1931620-1931670	BE2_C	brain:	n/a
15	chr5:1931620-1931670	ovcar-3	ovarian:	n/a
16	chr5:1934165-1934215	ECC-1	luminal epithelium:	n/a
17	chr5:1931544-1931594	AG10803	skin:	n/a
18	chr5:1925014-1925064	RPTEC	kidney:	n/a
19	chr5:1930928-1930978	NT2-D1	testis:	n/a
20	chr5:1931781-1931831	SK-N-SH	brain:	n/a
21	chr5:1925014-1925064	HPAEpiC	pulmonary alveolar:	n/a
22	chr5:1932098-1932148	Jurkat	blood:	n/a
23	chr5:1934165-1934215	ovcar-3	ovarian:	n/a
24	chr5:1931620-1931670	HAEpiC	amniotic membrane:	n/a
25	chr5:1934165-1934215	SAEC	small airway:	n/a
26	chr5:1931058-1931108	HL-60	blood:	n/a
27	chr5:1934165-1934215	ProgFib	skin:	n/a
28	chr5:1930928-1930978	AG10803	skin:	n/a
29	chr5:1930801-1930851	ovcar-3	ovarian:	n/a
30	chr5:1931376-1931426	BE2_C	brain:	n/a
31	chr5:1931058-1931108	HRPEpiC	eye:	n/a
32	chr5:1931376-1931426	MCF10A-Er-Src	breast:	n/a
33	chr5:1930928-1930978	GM12892	blood:	n/a
34	chr5:1931251-1931301	HCF	heart:	n/a
35	chr5:1930801-1930851	A549	lung:	n/a
36	chr5:1925014-1925064	AG09319	gingival:	n/a
37	chr5:1931544-1931594	PrEC	prostate:	n/a
38	chr5:1930801-1930851	HNPCEpiC	eye:	n/a
39	chr5:1931781-1931831	AoSMC	blood vessel:	n/a
40	chr5:1927225-1927275	HUVEC	blood vessel:	n/a
41	chr5:1931058-1931108	GM06990	blood:	n/a
42	chr5:1931376-1931426	ProgFib	skin:	n/a
43	chr5:1931376-1931426	RPTEC	kidney:	n/a
44	chr5:1931058-1931108	K562	blood:	n/a
45	chr5:1931376-1931426	HIPEpiC	eye:	n/a
46	chr5:1931544-1931594	SK-N-SH	brain:	n/a
47	chr5:1931376-1931426	AG10803	skin:	n/a
48	chr5:1925014-1925064	GM12878	blood:	n/a
49	chr5:1931781-1931831	GM12878	blood:	n/a
50	chr5:1930928-1930978	IMR90	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr5:1881423..1883600-chr5:1931817..1933419,2	MCF-7	breast:
2	chr5:1928752..1930799-chr5:1946292..1948777,2	MCF-7	breast:
3	chr5:1923598..1926065-chr5:2006441..2007973,2	K562	blood:
4	chr5:1920038..1922611-chr5:1924901..1927373,2	MCF-7	breast:
5	chr5:1922868..1925557-chr5:1925659..1927215,2	MCF-7	breast:
6	chr5:1922868..1925557-chr5:1925659..1927215,2	MCF-7	breast:
7	chr5:1881475..1885354-chr5:1933918..1938503,4	MCF-7	breast:
8	chr5:1923560..1925350-chr5:1937042..1939475,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IRX4-2	chr5:1929770-1930148	NONHSAT100080
2	lnc-NDUFS6-5	chr5:1933923-1934099	XLOC_004250
3	lnc-IRX4-2	chr5:1929182-1929710	NONHSAT100080
4	lnc-IRX4-2	chr5:1929007-1930243	XLOC_004707
5	lnc-NDUFS6-5	chr5:1931105-1931503	XLOC_004250
6	lnc-NDUFS6-5	chr5:1933977-1934099	XLOC_004250
7	lnc-NDUFS6-5	chr5:1931131-1931503	XLOC_004250
8	lnc-NDUFS6-5	chr5:1933923-1934099	XLOC_004250
9	lnc-NDUFS6-5	chr5:1931371-1931503	XLOC_004250
10	lnc-IRX4-2	chr5:1930518-1930577	XLOC_004707
11	lnc-NDUFS6-5	chr5:1933923-1934099	XLOC_004250
12	lnc-NDUFS6-5	chr5:1933923-1934099	XLOC_004250
13	lnc-NDUFS6-5	chr5:1931298-1931503	XLOC_004250

Variant related genes	Relation type
ENSG00000248994	TF binding region
ENSG00000248994	CpG island
ENSG00000113430	chromatin interactions
ENSG00000249116	chromatin interactions
PFAS	miRNA target sites
UTP15	miRNA target sites
UTRN	miRNA target sites
LEPRE1	miRNA target sites

Extended variants
information (count: 485 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:485 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568353367	chr5:1924828-1924829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs140621942	chr5:1924970-1924971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs552546023	chr5:1925011-1925012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs10036227	chr5:1925013-1925014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs571133667	chr5:1925041-1925042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs537043190	chr5:1925044-1925045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs540735595	chr5:1925193-1925194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs113032132	chr5:1925201-1925202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs111316690	chr5:1925202-1925203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs4478361	chr5:1925303-1925304	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs575058483	chr5:1925322-1925323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs539179061	chr5:1925329-1925330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs557408340	chr5:1925331-1925332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs552996515	chr5:1925346-1925347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs192383075	chr5:1925355-1925356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs574571042	chr5:1925379-1925380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs568023067	chr5:1925383-1925384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs574278287	chr5:1925391-1925392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs544551599	chr5:1925402-1925403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs563092691	chr5:1925431-1925432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs532047544	chr5:1925492-1925493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs184877195	chr5:1925505-1925506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs551950064	chr5:1925508-1925509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs560559087	chr5:1925519-1925520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs6890530	chr5:1925537-1925538	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs189253607	chr5:1925544-1925545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs192063712	chr5:1925562-1925563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs147470088	chr5:1925564-1925565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs550583898	chr5:1925585-1925586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs568737550	chr5:1925596-1925597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs539247224	chr5:1925647-1925648	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs557446381	chr5:1925666-1925667	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs557473682	chr5:1925748-1925749	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs373457703	chr5:1925757-1925758	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs572615752	chr5:1925784-1925785	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs529429588	chr5:1925797-1925798	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs533608897	chr5:1925799-1925800	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs555363091	chr5:1925801-1925802	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs573523337	chr5:1925807-1925808	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs139302717	chr5:1925808-1925809	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs563154729	chr5:1925920-1925921	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs576130490	chr5:1925959-1925960	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs578234706	chr5:1925961-1925962	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs372791775	chr5:1925981-1925982	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs377343103	chr5:1925999-1926000	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs11749860	chr5:1926026-1926027	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs115505085	chr5:1926028-1926029	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs549171673	chr5:1926105-1926106	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs138709181	chr5:1926131-1926132	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs376428037	chr5:1926134-1926135	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:114)

Disease	PMID	Source
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16608533	CNVD
Cervical cancer	16585170	CNVD
Glioblastoma multiforme	22286061	CNVD
Lung cancer	17925434	CNVD
Ovarian cancer	20844748	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Non-small cell lung cancer	21829676	CNVD
Intracranial ependymoma	16609018	CNVD
Breast cancer	19181860	CNVD
prenatal diagnosis	20453657	CNVD
Developmental delay	19490664	CNVD
Human papillomavirus	17975027	CNVD
Acute monocytic leukemia	16498392	CNVD
Gastric cancer	16891809	CNVD
Intracranial aneurysm	16715129	CNVD
Emphysema	19352772	CNVD
Chordoma	18071362	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Lung cancer	21911935	CNVD
Cri-du chat syndrome	21549014	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Sudden cardiac death	19188705	CNVD
renal disease	17924346	CNVD
abnormal development	18461090	CNVD
Lung cancer	19547694	CNVD
Cri-du chat syndrome	22283845	CNVD
Disorders of sex development	21048976	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Honadal dysgenesis	21048976	CNVD
Cancer	16751803	CNVD
Breast cancer	17133270	CNVD
Hepatocellular carcinoma	22174799	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Salivary gland tumor	18059337	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Kartagener syndrome	16639409	CNVD
Medulloblastoma	21979893	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	21364760	CNVD
Cancer	20164919	CNVD
Oral cancer	22144094	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Urothelial carcinoma	21177765	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Multiple myeloma	17550852	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Developmental delay	21147756	CNVD
prenatal diagnosis	22389664	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Breast cancer	21858162	CNVD
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Melanoma	22183965	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	22495311	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Schizophrenia	23813976	CNVD
Ependymoma	20639864	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:1924200-1928000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr5:1924400-1925600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr5:1925600-1926400	ZNF genes & repeats	Right Atrium	heart
4	chr5:1925600-1927600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr5:1925800-1926400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
6	chr5:1926000-1926200	Enhancers	Breast Myoepithelial Primary Cells	Breast
7	chr5:1926200-1929200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr5:1926400-1929200	Weak transcription	Right Atrium	heart
9	chr5:1926600-1927200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
10	chr5:1926800-1927000	Enhancers	H1 Cell Line	embryonic stem cell
11	chr5:1927000-1928000	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr5:1927200-1927800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr5:1927200-1928200	Enhancers	H9 Cell Line	embryonic stem cell
14	chr5:1927400-1928000	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr5:1927600-1928000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr5:1927800-1928000	Bivalent Enhancer	Fetal Muscle Leg	muscle
17	chr5:1927800-1928200	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr5:1927800-1930400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr5:1928000-1928200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr5:1928000-1928200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr5:1928000-1928200	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
22	chr5:1928000-1928200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr5:1928000-1928200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
24	chr5:1928000-1928200	Enhancers	Pancreas	Pancrea
25	chr5:1928000-1928400	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
26	chr5:1928000-1928400	Enhancers	H1 Cell Line	embryonic stem cell
27	chr5:1928000-1928400	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr5:1928000-1928400	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr5:1928000-1928400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr5:1928200-1928400	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
31	chr5:1928200-1928400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr5:1928200-1929200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr5:1928200-1929200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr5:1928200-1929200	Weak transcription	H9 Cell Line	embryonic stem cell
35	chr5:1928200-1929200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr5:1928200-1929200	Weak transcription	Esophagus	oesophagus
37	chr5:1928200-1929200	Weak transcription	Pancreas	Pancrea
38	chr5:1928400-1929400	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr5:1928400-1930400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr5:1928800-1930000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr5:1929000-1929200	Weak transcription	Gastric	stomach
42	chr5:1929200-1929600	Flanking Bivalent TSS/Enh	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr5:1929200-1929600	Genic enhancers	Gastric	stomach
44	chr5:1929200-1929800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr5:1929200-1930000	ZNF genes & repeats	Spleen	Spleen
46	chr5:1929200-1930200	Enhancers	Breast Myoepithelial Primary Cells	Breast
47	chr5:1929200-1930200	Genic enhancers	Esophagus	oesophagus
48	chr5:1929200-1930400	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr5:1929200-1930400	Bivalent/Poised TSS	Fetal Lung	lung
50	chr5:1929200-1930400	Enhancers	Pancreas	Pancrea

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