Variant report

Variant	nsv1034638
Chromosome Location	chr4:187185385-187213477
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	ARID3A	chr4:187187688-187188343	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:187186808-187187453	HepG2	liver:	n/a	n/a
3	ATF1	chr4:187212412-187212640	K562	blood:	n/a	n/a
4	BCL3	chr4:187206252-187206646	GM12878	blood:	n/a	n/a
5	BCL3	chr4:187206290-187206632	GM12878	blood:	n/a	n/a
6	BCL3	chr4:187204147-187204479	GM12878	blood:	n/a	n/a
7	CEBPB	chr4:187199698-187199972	IMR90	lung:	n/a	n/a
8	CEBPB	chr4:187197049-187197207	A549	lung:	n/a	n/a
9	CEBPB	chr4:187187997-187188270	HepG2	liver:	n/a	n/a
10	CEBPB	chr4:187199637-187200010	HepG2	liver:	n/a	n/a
11	CEBPB	chr4:187194311-187194483	IMR90	lung:	n/a	n/a
12	CEBPB	chr4:187187995-187188231	IMR90	lung:	n/a	n/a
13	CEBPB	chr4:187199707-187199949	A549	lung:	n/a	n/a
14	CEBPB	chr4:187186894-187187383	HepG2	liver:	n/a	n/a
15	CEBPB	chr4:187199733-187199876	HepG2	liver:	n/a	n/a
16	CEBPB	chr4:187199658-187199935	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr4:187205777-187205990	HepG2	liver:	n/a	chr4:187205877-187205888
18	CEBPB	chr4:187199769-187199908	K562	blood:	n/a	n/a
19	CTCF	chr4:187206482-187206541	GM19239	blood:	n/a	n/a
20	CUX1	chr4:187187701-187187730	K562	blood:	n/a	n/a
21	E2F4	chr4:187196152-187196281	MCF10A-Er-Src	breast:	n/a	n/a
22	ELF1	chr4:187187846-187188175	HepG2	liver:	n/a	chr4:187188015-187188027
23	ELF1	chr4:187187923-187188181	HepG2	liver:	n/a	chr4:187188015-187188027
24	EP300	chr4:187186763-187187218	HepG2	liver:	n/a	n/a
25	EP300	chr4:187186702-187187485	HepG2	liver:	n/a	n/a
26	FOXA1	chr4:187186763-187187209	HepG2	liver:	n/a	n/a
27	FOXA1	chr4:187186747-187187536	HepG2	liver:	n/a	n/a
28	FOXA1	chr4:187205834-187206143	HepG2	liver:	n/a	n/a
29	FOXA1	chr4:187204428-187204782	HepG2	liver:	n/a	n/a
30	FOXA1	chr4:187204476-187204782	HepG2	liver:	n/a	n/a
31	FOXA1	chr4:187186748-187187286	HepG2	liver:	n/a	n/a
32	FOXA1	chr4:187204332-187204853	HepG2	liver:	n/a	n/a
33	FOXA1	chr4:187204383-187204858	HepG2	liver:	n/a	n/a
34	FOXA1	chr4:187186834-187187179	HepG2	liver:	n/a	n/a
35	FOXA2	chr4:187204481-187204811	HepG2	liver:	n/a	n/a
36	FOXA2	chr4:187186836-187187238	HepG2	liver:	n/a	n/a
37	FOXA2	chr4:187212371-187212588	HepG2	liver:	n/a	chr4:187212466-187212478
38	GATA3	chr4:187188381-187188690	SH-SY5Y	brain:	n/a	chr4:187188439-187188449
39	GTF2F1	chr4:187187836-187188073	H1-hESC	embryonic stem cell:	n/a	n/a
40	HDAC2	chr4:187187891-187188190	HepG2	liver:	n/a	n/a
41	HDAC2	chr4:187186783-187187244	HepG2	liver:	n/a	chr4:187186816-187186830 chr4:187186813-187186827 chr4:187186817-187186831 chr4:187186820-187186834
42	HEY1	chr4:187186733-187187653	HepG2	liver:	n/a	n/a
43	HEY1	chr4:187187720-187188282	HepG2	liver:	n/a	n/a
44	HEY1	chr4:187186751-187187810	HepG2	liver:	n/a	n/a
45	HEY1	chr4:187187820-187188192	HepG2	liver:	n/a	n/a
46	HNF4A	chr4:187186772-187187174	HepG2	liver:	n/a	chr4:187186929-187186944
47	HNF4A	chr4:187204395-187204800	HepG2	liver:	n/a	chr4:187204633-187204655 chr4:187204637-187204651 chr4:187204638-187204650 chr4:187204639-187204651 chr4:187204637-187204650 chr4:187204638-187204650 chr4:187204637-187204650 chr4:187204636-187204651 chr4:187204638-187204650 chr4:187204637-187204651 chr4:187204642-187204654 chr4:187204637-187204651 chr4:187204581-187204596 chr4:187204635-187204653 chr4:187204637-187204650 chr4:187204638-187204651 chr4:187204638-187204650
48	HNF4A	chr4:187204449-187204767	HepG2	liver:	n/a	chr4:187204633-187204655 chr4:187204637-187204651 chr4:187204638-187204650 chr4:187204639-187204651 chr4:187204637-187204650 chr4:187204638-187204650 chr4:187204637-187204650 chr4:187204636-187204651 chr4:187204638-187204650 chr4:187204637-187204651 chr4:187204642-187204654 chr4:187204637-187204651 chr4:187204581-187204596 chr4:187204635-187204653 chr4:187204637-187204650 chr4:187204638-187204651 chr4:187204638-187204650
49	HNF4A	chr4:187186777-187187178	HepG2	liver:	n/a	chr4:187186929-187186944
50	HNF4G	chr4:187204488-187204826	HepG2	liver:	n/a	chr4:187204633-187204655 chr4:187204637-187204651 chr4:187204638-187204650 chr4:187204639-187204651 chr4:187204637-187204650 chr4:187204638-187204650 chr4:187204637-187204650 chr4:187204638-187204650 chr4:187204637-187204651 chr4:187204642-187204654 chr4:187204637-187204651 chr4:187204635-187204653 chr4:187204635-187204650 chr4:187204637-187204650 chr4:187204638-187204651 chr4:187204638-187204650

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:187192322-187192372	SK-N-MC	brain:	n/a
2	chr4:187192322-187192372	SK-N-MC	brain:	n/a
3	chr4:187209867-187209917	AG09309	skin:	n/a
4	chr4:187186949-187186999	SAEC	small airway:	n/a
5	chr4:187204810-187204860	Hepatocyte	liver:	n/a
6	chr4:187186953-187187003	BJ	skin:	n/a
7	chr4:187186265-187186315	AoSMC	blood vessel:	n/a
8	chr4:187186953-187187003	HPAEpiC	pulmonary alveolar:	n/a
9	chr4:187204810-187204860	HRE	kidney:	n/a
10	chr4:187204810-187204860	BJ	skin:	n/a
11	chr4:187186949-187186999	AG04450	lung:	fetal
12	chr4:187187177-187187227	Hepatocyte	liver:	n/a
13	chr4:187186949-187186999	HEK293	kidney:	embryo
14	chr4:187186949-187186999	MCF-7	breast:	n/a
15	chr4:187186949-187186999	K562	blood:	n/a
16	chr4:187186949-187186999	HAEpiC	amniotic membrane:	n/a
17	chr4:187204810-187204860	HIPEpiC	eye:	n/a
18	chr4:187209867-187209917	HCM	heart:	n/a
19	chr4:187185997-187186047	Hela-S3	cervix:	n/a
20	chr4:187185997-187186047	HMEC	breast:	n/a
21	chr4:187204810-187204860	SK-N-SH_RA	brain:	n/a
22	chr4:187185716-187185766	LNCaP	prostate:	n/a
23	chr4:187186265-187186315	CMK	blood:	n/a
24	chr4:187186953-187187003	MCF10A-Er-Src	breast:	n/a
25	chr4:187185997-187186047	PrEC	prostate:	n/a
26	chr4:187209867-187209917	NB4	blood:	n/a
27	chr4:187187177-187187227	RPTEC	kidney:	n/a
28	chr4:187209867-187209917	NT2-D1	testis:	n/a
29	chr4:187187177-187187227	HEK293	kidney:	embryo
30	chr4:187185716-187185766	HAEpiC	amniotic membrane:	n/a
31	chr4:187187177-187187227	LNCaP	prostate:	n/a
32	chr4:187192322-187192372	NH-A	brain:	n/a
33	chr4:187186265-187186315	HRPEpiC	eye:	n/a
34	chr4:187186949-187186999	ECC-1	luminal epithelium:	n/a
35	chr4:187186265-187186315	NHBE	bronchial:	n/a
36	chr4:187187177-187187227	HCM	heart:	n/a
37	chr4:187185716-187185766	MCF10A-Er-Src	breast:	n/a
38	chr4:187185997-187186047	GM12891	blood:	n/a
39	chr4:187204810-187204860	CMK	blood:	n/a
40	chr4:187185997-187186047	AoSMC	blood vessel:	n/a
41	chr4:187185997-187186047	PFSK-1	brain:	n/a
42	chr4:187204810-187204860	ECC-1	luminal epithelium:	n/a
43	chr4:187186949-187186999	H1-hESC	embryonic stem cell:	embryo
44	chr4:187185716-187185766	BJ	skin:	n/a
45	chr4:187186949-187186999	HepG2	liver:	n/a
46	chr4:187204810-187204860	HPAEpiC	pulmonary alveolar:	n/a
47	chr4:187204810-187204860	HL-60	blood:	n/a
48	chr4:187187177-187187227	NHDF-neo	bronchial:	n/a
49	chr4:187187177-187187227	HCPEpiC	choroid plexus:	n/a
50	chr4:187192322-187192372	GM19239	blood:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:187196134..187198336-chr4:187202703..187204992,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KLKB1-2	chr4:187187127-187187943	NONHSAT099651
2	lnc-MTNR1A-7	chr4:187213263-187213678	NONHSAT099654

Variant related genes	Relation type
F11	TF binding region
F11	CpG island
ENSG00000088926	chromatin interactions

Extended variants
information (count: 1271 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:1271 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3756008	chr4:187185385-187185386	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	disease
2	rs555610974	chr4:187185477-187185478	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs142867288	chr4:187185533-187185534	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs370299994	chr4:187185567-187185568	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs150996236	chr4:187185640-187185641	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs576039650	chr4:187185647-187185648	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs35610571	chr4:187185665-187185666	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs541469018	chr4:187185717-187185718	Enhancers Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
9	rs140986092	chr4:187185729-187185730	Enhancers Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
10	rs528006170	chr4:187185769-187185770	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs547669396	chr4:187185908-187185909	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs144918963	chr4:187185945-187185946	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs533384385	chr4:187185953-187185954	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs181708024	chr4:187185998-187185999	Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
15	rs186243619	chr4:187186011-187186012	Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
16	rs570063043	chr4:187186028-187186029	Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
17	rs4253809	chr4:187186049-187186050	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs535937723	chr4:187186050-187186051	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs3756009	chr4:187186111-187186112	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs4253392	chr4:187186112-187186113	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs566054597	chr4:187186118-187186119	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs190662485	chr4:187186134-187186135	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs554121778	chr4:187186140-187186141	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs4253810	chr4:187186143-187186144	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs183216901	chr4:187186171-187186172	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs539259538	chr4:187186176-187186177	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs562949616	chr4:187186191-187186192	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs4253393	chr4:187186201-187186202	Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs545875862	chr4:187186258-187186259	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs111823325	chr4:187186266-187186267	Flanking Active TSS Enhancers Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
31	rs549805000	chr4:187186329-187186330	Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs4253811	chr4:187186356-187186357	Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs59309284	chr4:187186367-187186368	Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs561381768	chr4:187186370-187186371	Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs4253394	chr4:187186372-187186373	Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs140379339	chr4:187186381-187186382	Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs74962579	chr4:187186511-187186512	Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs4253812	chr4:187186530-187186531	Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs533632265	chr4:187186544-187186545	Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs554137099	chr4:187186547-187186548	Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs386683493	chr4:187186548-187186549	Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs3836617	chr4:187186549-187186550	Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs369327834	chr4:187186553-187186554	Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs60567977	chr4:187186554-187186555	Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs532613192	chr4:187186558-187186559	Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs397841169	chr4:187186559-187186560	Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs563900393	chr4:187186564-187186565	Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs529393825	chr4:187186601-187186602	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs549486308	chr4:187186629-187186630	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs187979051	chr4:187186644-187186645	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	21785460	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20581869	CNVD
Hepatocellular carcinoma	16750200	CNVD
abnormal development	18461090	CNVD
Neuroblastoma	16790693	CNVD
Colorectal cancer	16774939	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Basal cell lymphoma	17053054	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Lung adenocarcinoma	17086460	CNVD
Facioscapulohumeral muscular dystrophy	21829175	CNVD
Disorders of sex development	21048976	CNVD
Ovarian cancer	20844748	CNVD
Autism	18414403	CNVD
Urothelial carcinoma	21177765	CNVD
Cancer	20164920	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	20409316	CNVD
Rhabdomyosarcoma	16790082	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:159 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:187149800-187186800	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr4:187150200-187187200	Weak transcription	Duodenum Smooth Muscle	Duodenum
3	chr4:187151000-187187200	Weak transcription	Colon Smooth Muscle	Colon
4	chr4:187177400-187191800	Weak transcription	Right Atrium	heart
5	chr4:187180000-187185400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr4:187180200-187185800	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr4:187180400-187185600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
8	chr4:187182200-187185400	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr4:187182200-187185600	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr4:187182200-187186000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr4:187182200-187187600	Weak transcription	Fetal Lung	lung
12	chr4:187182400-187185400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr4:187182400-187185800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr4:187182600-187185400	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr4:187182600-187186000	Weak transcription	Fetal Intestine Large	intestine
16	chr4:187183000-187185400	Weak transcription	Fetal Intestine Small	intestine
17	chr4:187183000-187186000	Weak transcription	Pancreas	Pancrea
18	chr4:187184000-187186800	Enhancers	Liver	Liver
19	chr4:187185200-187186800	Enhancers	HepG2	liver
20	chr4:187185200-187187000	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr4:187185400-187185600	Enhancers	Fetal Intestine Small	intestine
22	chr4:187185400-187186200	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr4:187185400-187186400	Enhancers	H1 Cell Line	embryonic stem cell
24	chr4:187185400-187187000	Enhancers	H9 Cell Line	embryonic stem cell
25	chr4:187185400-187187000	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr4:187185600-187186000	Weak transcription	Fetal Intestine Small	intestine
27	chr4:187185600-187186800	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr4:187185600-187186800	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr4:187185800-187186400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr4:187185800-187186600	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr4:187186000-187186400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr4:187186000-187187000	Enhancers	Pancreas	Pancrea
33	chr4:187186000-187187200	Enhancers	Fetal Intestine Large	intestine
34	chr4:187186000-187187600	Enhancers	Fetal Intestine Small	intestine
35	chr4:187186000-187188200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr4:187186200-187186400	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
37	chr4:187186200-187187000	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr4:187186400-187186800	Weak transcription	Duodenum Mucosa	Duodenum
39	chr4:187186400-187187000	Weak transcription	H1 Cell Line	embryonic stem cell
40	chr4:187186400-187188200	Active TSS	ES-I3 Cell Line	embryonic stem cell
41	chr4:187186600-187188600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
42	chr4:187186800-187187000	Flanking Active TSS	Liver	Liver
43	chr4:187186800-187187000	Flanking Active TSS	HepG2	liver
44	chr4:187186800-187187400	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr4:187186800-187187800	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
46	chr4:187186800-187188000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr4:187186800-187188200	Active TSS	Pancreatic Islets	Pancreatic Islet
48	chr4:187186800-187188400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr4:187186800-187188400	Enhancers	Cortex derived primary cultured neurospheres	brain
50	chr4:187186800-187188600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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