Variant report

Variant	esv3362028
Chromosome Location	chr4:3574854-3587452
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:120)
CpG islands
(count:430)
Chromatin interactive
region (count:7)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:120 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr4:3576432-3576518	K562	blood:	n/a	n/a
2	BHLHE40	chr4:3586629-3586990	HepG2	liver:	n/a	n/a
3	BHLHE40	chr4:3587360-3587604	K562	blood:	n/a	n/a
4	BRCA1	chr4:3576365-3576373	HepG2	liver:	n/a	n/a
5	BRCA1	chr4:3578147-3578290	HepG2	liver:	n/a	n/a
6	CEBPB	chr4:3578250-3578520	HepG2	liver:	n/a	n/a
7	CEBPB	chr4:3576042-3576167	HepG2	liver:	n/a	chr4:3576093-3576104
8	CEBPB	chr4:3578297-3578444	HepG2	liver:	n/a	n/a
9	CHD2	chr4:3577950-3577961	K562	blood:	n/a	n/a
10	CHD2	chr4:3578272-3578287	HepG2	liver:	n/a	n/a
11	CHD2	chr4:3575147-3575242	HepG2	liver:	n/a	n/a
12	CTCF	chr4:3582500-3582650	BE2_C	brain:	n/a	n/a
13	CTCF	chr4:3575560-3575710	GM12872	blood:	n/a	n/a
14	CTCF	chr4:3586347-3586401	Kidney_OC	kidney:	n/a	n/a
15	CTCF	chr4:3580840-3580990	GM12871	blood:	n/a	n/a
16	CTCF	chr4:3582880-3583030	HEEpiC	esophagus:	n/a	n/a
17	CTCF	chr4:3582480-3582630	BE2_C	brain:	n/a	n/a
18	CTCF	chr4:3582760-3582910	HepG2	liver:	n/a	n/a
19	CTCF	chr4:3575797-3575851	GM10248	blood:	n/a	n/a
20	CTCF	chr4:3585797-3585872	GM19239	blood:	n/a	n/a
21	CTCF	chr4:3582720-3582870	BE2_C	brain:	n/a	n/a
22	CTCF	chr4:3581060-3581210	AG09319	gingival:	n/a	n/a
23	CTCF	chr4:3575913-3576104	K562	blood:	n/a	n/a
24	EGR1	chr4:3577210-3577484	K562	blood:	n/a	chr4:3577308-3577319 chr4:3577307-3577321 chr4:3577308-3577319 chr4:3577309-3577319 chr4:3577307-3577320 chr4:3577309-3577319 chr4:3577307-3577320
25	EGR1	chr4:3577259-3577383	K562	blood:	n/a	chr4:3577308-3577319 chr4:3577307-3577321 chr4:3577308-3577319 chr4:3577309-3577319 chr4:3577307-3577320 chr4:3577309-3577319 chr4:3577307-3577320
26	EGR1	chr4:3582602-3582923	ECC-1	luminal epithelium:	n/a	chr4:3582712-3582726 chr4:3582714-3582724
27	EGR1	chr4:3582506-3582862	K562	blood:	n/a	chr4:3582712-3582726 chr4:3582714-3582724
28	ELF1	chr4:3587306-3587633	HepG2	liver:	n/a	n/a
29	ELF1	chr4:3587249-3587646	K562	blood:	n/a	n/a
30	ELF1	chr4:3587254-3587686	HepG2	liver:	n/a	n/a
31	EP300	chr4:3582648-3582995	SK-N-SH_RA	brain:	n/a	n/a
32	EP300	chr4:3581734-3581817	GM12878	blood:	n/a	n/a
33	EP300	chr4:3587274-3587622	SK-N-SH_RA	brain:	n/a	n/a
34	EP300	chr4:3587300-3587648	K562	blood:	n/a	n/a
35	EP300	chr4:3587256-3587685	SK-N-SH_RA	brain:	n/a	n/a
36	ESR1	chr4:3577077-3578029	ECC-1	luminal epithelium:	n/a	n/a
37	ESR1	chr4:3577165-3577525	ECC-1	luminal epithelium:	n/a	n/a
38	ESR1	chr4:3577021-3578004	ECC-1	luminal epithelium:	n/a	n/a
39	ESR1	chr4:3577190-3577439	ECC-1	luminal epithelium:	n/a	n/a
40	ESR1	chr4:3577093-3577958	ECC-1	luminal epithelium:	n/a	n/a
41	FOS	chr4:3582773-3582881	MCF10A-Er-Src	breast:	n/a	n/a
42	FOXA1	chr4:3586652-3586952	HepG2	liver:	n/a	n/a
43	FOXA1	chr4:3586639-3586907	HepG2	liver:	n/a	n/a
44	FOXA1	chr4:3587152-3587707	HepG2	liver:	n/a	n/a
45	FOXA1	chr4:3586512-3587056	HepG2	liver:	n/a	n/a
46	FOXA1	chr4:3586649-3586947	HepG2	liver:	n/a	n/a
47	FOXA1	chr4:3587141-3587631	HepG2	liver:	n/a	n/a
48	FOXA1	chr4:3587156-3587629	HepG2	liver:	n/a	n/a
49	FOXA1	chr4:3587273-3587626	HepG2	liver:	n/a	n/a
50	FOXA2	chr4:3586655-3586954	HepG2	liver:	n/a	n/a

(count:430 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:3576336-3576386	HRCEpiC	kidney:	n/a
2	chr4:3577650-3577700	BE2_C	brain:	n/a
3	chr4:3577650-3577700	SK-N-SH_RA	brain:	n/a
4	chr4:3576336-3576386	HRCEpiC	kidney:	n/a
5	chr4:3577650-3577700	BE2_C	brain:	n/a
6	chr4:3577650-3577700	SK-N-SH_RA	brain:	n/a
7	chr4:3578583-3578633	PFSK-1	brain:	n/a
8	chr4:3576336-3576386	HEK293	kidney:	embryo
9	chr4:3578583-3578633	T-47D	breast:	n/a
10	chr4:3577650-3577700	GM12878	blood:	n/a
11	chr4:3578432-3578482	ECC-1	luminal epithelium:	n/a
12	chr4:3576489-3576539	PANC-1	pancreas:	n/a
13	chr4:3576489-3576539	PFSK-1	brain:	n/a
14	chr4:3577496-3577546	AG04450	lung:	fetal
15	chr4:3578432-3578482	HIPEpiC	eye:	n/a
16	chr4:3576273-3576323	RPTEC	kidney:	n/a
17	chr4:3578432-3578482	SK-N-SH	brain:	n/a
18	chr4:3578432-3578482	H1-hESC	embryonic stem cell:	embryo
19	chr4:3578583-3578633	NH-A	brain:	n/a
20	chr4:3576336-3576386	RPTEC	kidney:	n/a
21	chr4:3576273-3576323	LNCaP	prostate:	n/a
22	chr4:3576273-3576323	BE2_C	brain:	n/a
23	chr4:3577496-3577546	Hepatocyte	liver:	n/a
24	chr4:3577496-3577546	HRCEpiC	kidney:	n/a
25	chr4:3577650-3577700	SK-N-SH	brain:	n/a
26	chr4:3576336-3576386	K562	blood:	n/a
27	chr4:3577496-3577546	HCM	heart:	n/a
28	chr4:3576489-3576539	AoSMC	blood vessel:	n/a
29	chr4:3576336-3576386	HUVEC	blood vessel:	n/a
30	chr4:3577496-3577546	AG09309	skin:	n/a
31	chr4:3576336-3576386	Hepatocyte	liver:	n/a
32	chr4:3576273-3576323	Jurkat	blood:	n/a
33	chr4:3576489-3576539	T-47D	breast:	n/a
34	chr4:3578432-3578482	IMR90	lung:	fetal
35	chr4:3577650-3577700	HepG2	liver:	n/a
36	chr4:3578432-3578482	AG04450	lung:	fetal
37	chr4:3576273-3576323	PANC-1	pancreas:	n/a
38	chr4:3576489-3576539	HUVEC	blood vessel:	n/a
39	chr4:3576273-3576323	HIPEpiC	eye:	n/a
40	chr4:3577650-3577700	ProgFib	skin:	n/a
41	chr4:3578432-3578482	T-47D	breast:	n/a
42	chr4:3576273-3576323	HRCEpiC	kidney:	n/a
43	chr4:3576336-3576386	HRPEpiC	eye:	n/a
44	chr4:3576489-3576539	SK-N-SH_RA	brain:	n/a
45	chr4:3576273-3576323	CMK	blood:	n/a
46	chr4:3576489-3576539	NHDF-neo	bronchial:	n/a
47	chr4:3578432-3578482	HCM	heart:	n/a
48	chr4:3576336-3576386	NH-A	brain:	n/a
49	chr4:3576273-3576323	HNPCEpiC	eye:	n/a
50	chr4:3578432-3578482	HRCEpiC	kidney:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:3574894..3577613-chr4:3578076..3580368,2	K562	blood:
2	chr4:3532775..3535041-chr4:3574379..3576145,2	K562	blood:
3	chr4:3576753..3579179-chr4:3579407..3585070,6	K562	blood:
4	chr4:3577226..3578815-chr4:3583775..3586576,2	K562	blood:
5	chr4:3573176..3575691-chr4:3650301..3652396,2	MCF-7	breast:
6	chr4:3577022..3579696-chr4:3767335..3769205,3	MCF-7	breast:
7	chr4:3533888..3535501-chr4:3581402..3583969,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP3-368B9.1.1-1	chr4:3578596-3578850	NR_040045
2	lnc-RP3-368B9.1.1-1	chr4:3578596-3578850	XLOC_003428
3	lnc-RP3-368B9.1.1-1	chr4:3578596-3578850	XLOC_003428

No data

Variant related genes	Relation type
LINC00955	TF binding region
LINC00955	CpG island
ENSG00000216560	chromatin interactions
ENSG00000184160	chromatin interactions
ENSG00000163956	chromatin interactions
TMEM2	miRNA target sites

Extended variants
information (count: 934 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:934 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs544267515	chr4:3574859-3574860	ZNF genes & repeats Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs1741559	chr4:3574864-3574865	ZNF genes & repeats Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs561327698	chr4:3574872-3574873	ZNF genes & repeats Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs386670706	chr4:3574874-3574875	ZNF genes & repeats Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs77953035	chr4:3574875-3574876	ZNF genes & repeats Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs77128813	chr4:3574882-3574883	ZNF genes & repeats Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs560497405	chr4:3574904-3574905	ZNF genes & repeats Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs532647769	chr4:3574906-3574907	ZNF genes & repeats Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs1730810	chr4:3574925-3574926	ZNF genes & repeats Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs73199307	chr4:3574983-3574984	ZNF genes & repeats Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs552190073	chr4:3574989-3574990	ZNF genes & repeats Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs568880841	chr4:3574990-3574991	ZNF genes & repeats Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs73199308	chr4:3574991-3574992	ZNF genes & repeats Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs548621113	chr4:3574992-3574993	ZNF genes & repeats Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs71202513	chr4:3574998-3574999	ZNF genes & repeats Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs73199309	chr4:3575008-3575009	ZNF genes & repeats Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs568450995	chr4:3575013-3575014	ZNF genes & repeats Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs73199310	chr4:3575034-3575035	ZNF genes & repeats Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs77988627	chr4:3575057-3575058	ZNF genes & repeats Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs79637984	chr4:3575061-3575062	ZNF genes & repeats Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs76219117	chr4:3575065-3575066	ZNF genes & repeats Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs536491728	chr4:3575068-3575069	ZNF genes & repeats Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs75492680	chr4:3575074-3575075	ZNF genes & repeats Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs73199311	chr4:3575097-3575098	ZNF genes & repeats Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs73199312	chr4:3575098-3575099	ZNF genes & repeats Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs538895499	chr4:3575104-3575105	ZNF genes & repeats Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs187804405	chr4:3575132-3575133	ZNF genes & repeats Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs114895281	chr4:3575136-3575137	ZNF genes & repeats Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs558589973	chr4:3575151-3575152	ZNF genes & repeats Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs66847916	chr4:3575156-3575157	ZNF genes & repeats Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs75063002	chr4:3575171-3575172	ZNF genes & repeats Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs10050197	chr4:3575172-3575173	ZNF genes & repeats Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs73084761	chr4:3575218-3575219	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs67101169	chr4:3575285-3575286	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs371767061	chr4:3575299-3575300	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs79086176	chr4:3575301-3575302	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs141315223	chr4:3575307-3575308	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs75960748	chr4:3575310-3575311	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs115850554	chr4:3575311-3575312	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs74193450	chr4:3575315-3575316	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs374735258	chr4:3575316-3575317	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs368033203	chr4:3575317-3575318	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs371878453	chr4:3575325-3575326	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs375548249	chr4:3575326-3575327	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs200342425	chr4:3575328-3575329	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs369928088	chr4:3575330-3575331	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs371964989	chr4:3575331-3575332	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs575283895	chr4:3575334-3575335	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs181151335	chr4:3575336-3575337	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs543986709	chr4:3575337-3575338	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Retinitis pigmentosa	18421352	CNVD
Wolf-Hirschhorn syndrome	19259404	CNVD
Bladder cancer	19242612	CNVD
Breast cancer	19242612	CNVD
Congenital anomalies of the kidney and urinary tract	19242612	CNVD
abnormal development	18461090	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	21544195	CNVD
Melanoma	20688739	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Ependymoma	20639864	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:106 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:3550600-3580400	Weak transcription	Right Atrium	heart
2	chr4:3573000-3575600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr4:3573000-3580200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
4	chr4:3573800-3578200	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr4:3574600-3575200	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr4:3575200-3576400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr4:3575600-3575800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
8	chr4:3576000-3579600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr4:3576400-3576600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr4:3576400-3576600	Enhancers	Gastric	stomach
11	chr4:3576600-3577600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr4:3576600-3580200	Weak transcription	Gastric	stomach
13	chr4:3576800-3578600	Enhancers	Fetal Intestine Large	intestine
14	chr4:3577000-3577200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr4:3577000-3577200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr4:3577000-3578600	Enhancers	Fetal Intestine Small	intestine
17	chr4:3577200-3577400	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr4:3577200-3577400	Bivalent Enhancer	HepG2	liver
19	chr4:3577400-3577600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr4:3577400-3577800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
21	chr4:3577400-3578000	Flanking Bivalent TSS/Enh	HepG2	liver
22	chr4:3577600-3577800	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr4:3577600-3577800	Bivalent Enhancer	Right Ventricle	heart
24	chr4:3577600-3578800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr4:3577800-3578200	Enhancers	Duodenum Mucosa	Duodenum
26	chr4:3578000-3578400	Bivalent Enhancer	Stomach Smooth Muscle	stomach
27	chr4:3578000-3578600	Flanking Active TSS	HepG2	liver
28	chr4:3578200-3578400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr4:3578200-3578400	Weak transcription	Duodenum Mucosa	Duodenum
30	chr4:3578400-3578800	ZNF genes & repeats	Duodenum Mucosa	Duodenum
31	chr4:3578400-3579000	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
32	chr4:3578600-3578800	Active TSS	Fetal Intestine Large	intestine
33	chr4:3578600-3578800	Bivalent Enhancer	Fetal Muscle Leg	muscle
34	chr4:3578600-3579200	Bivalent Enhancer	Stomach Smooth Muscle	stomach
35	chr4:3578600-3579400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr4:3578600-3579400	Enhancers	HepG2	liver
37	chr4:3578600-3579600	Flanking Active TSS	Fetal Intestine Small	intestine
38	chr4:3578800-3579000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr4:3578800-3579000	Flanking Active TSS	Fetal Intestine Large	intestine
40	chr4:3578800-3579400	Active TSS	Duodenum Mucosa	Duodenum
41	chr4:3578800-3579400	Bivalent Enhancer	Right Ventricle	heart
42	chr4:3579000-3579200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
43	chr4:3579000-3579600	Active TSS	Fetal Intestine Large	intestine
44	chr4:3579400-3580000	Weak transcription	Duodenum Mucosa	Duodenum
45	chr4:3579400-3582200	Weak transcription	HepG2	liver
46	chr4:3579600-3580400	ZNF genes & repeats	Fetal Intestine Large	intestine
47	chr4:3579600-3580600	Enhancers	Fetal Intestine Small	intestine
48	chr4:3579600-3580800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr4:3580000-3580600	ZNF genes & repeats	Duodenum Mucosa	Duodenum
50	chr4:3580200-3580600	ZNF genes & repeats	Gastric	stomach

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