Variant report

Variant	esv1831682
Chromosome Location	chr4:91979094-92114281
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	chr4:92034335-92034619	HepG2	liver:	n/a	n/a
2	BACH1	chr4:92007259-92007496	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr4:91983060-91983121	K562	blood:	n/a	n/a
4	BCL11A	chr4:92010407-92010604	GM12878	blood:	n/a	n/a
5	BCL11A	chr4:92010328-92010676	GM12878	blood:	n/a	n/a
6	BRCA1	chr4:91985692-91985806	H1-hESC	embryonic stem cell:	n/a	n/a
7	CBX3	chr4:92024996-92025295	K562	blood:	n/a	n/a
8	CEBPB	chr4:92044571-92044854	HepG2	liver:	n/a	chr4:92044758-92044769 chr4:92044718-92044729
9	CEBPB	chr4:92061857-92062184	IMR90	lung:	n/a	chr4:92062016-92062027
10	CEBPB	chr4:92044637-92044818	H1-hESC	embryonic stem cell:	n/a	chr4:92044758-92044769 chr4:92044718-92044729
11	CEBPB	chr4:91986318-91986568	ECC-1	luminal epithelium:	n/a	chr4:91986482-91986491 chr4:91986482-91986491 chr4:91986482-91986491 chr4:91986470-91986483 chr4:91986480-91986493 chr4:91986480-91986491 chr4:91986480-91986493
12	CEBPB	chr4:92063703-92064031	HepG2	liver:	n/a	chr4:92063859-92063870
13	CEBPB	chr4:91986328-91986660	HepG2	liver:	n/a	chr4:91986482-91986491 chr4:91986482-91986491 chr4:91986482-91986491 chr4:91986470-91986483 chr4:91986480-91986493 chr4:91986480-91986491 chr4:91986480-91986493
14	CEBPB	chr4:92061834-92062206	HepG2	liver:	n/a	chr4:92062016-92062027
15	CEBPB	chr4:92034320-92034601	ECC-1	luminal epithelium:	n/a	n/a
16	CEBPB	chr4:92061869-92062156	K562	blood:	n/a	chr4:92062016-92062027
17	CEBPB	chr4:92044617-92044895	A549	lung:	n/a	chr4:92044758-92044769 chr4:92044718-92044729
18	CEBPB	chr4:91986304-91986629	H1-hESC	embryonic stem cell:	n/a	chr4:91986482-91986491 chr4:91986482-91986491 chr4:91986482-91986491 chr4:91986470-91986483 chr4:91986480-91986493 chr4:91986480-91986491 chr4:91986480-91986493
19	CEBPB	chr4:91986309-91986630	IMR90	lung:	n/a	chr4:91986482-91986491 chr4:91986482-91986491 chr4:91986482-91986491 chr4:91986470-91986483 chr4:91986480-91986493 chr4:91986480-91986491 chr4:91986480-91986493
20	CEBPB	chr4:92061856-92062186	A549	lung:	n/a	chr4:92062016-92062027
21	CEBPB	chr4:92063745-92063988	A549	lung:	n/a	chr4:92063859-92063870
22	CEBPB	chr4:91986316-91986672	K562	blood:	n/a	chr4:91986482-91986491 chr4:91986482-91986491 chr4:91986482-91986491 chr4:91986470-91986483 chr4:91986480-91986493 chr4:91986480-91986491 chr4:91986480-91986493
23	CEBPB	chr4:91985688-91986668	Hela-S3	cervix:	n/a	chr4:91986482-91986491 chr4:91986482-91986491 chr4:91986482-91986491 chr4:91986470-91986483 chr4:91986480-91986493 chr4:91986480-91986491 chr4:91986480-91986493
24	CEBPB	chr4:92063832-92063977	H1-hESC	embryonic stem cell:	n/a	chr4:92063859-92063870
25	CEBPB	chr4:92063721-92064028	IMR90	lung:	n/a	chr4:92063859-92063870
26	CEBPB	chr4:91986317-91986593	A549	lung:	n/a	chr4:91986482-91986491 chr4:91986482-91986491 chr4:91986482-91986491 chr4:91986470-91986483 chr4:91986480-91986493 chr4:91986480-91986491 chr4:91986480-91986493
27	CEBPB	chr4:92007232-92007488	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPZ	chr4:92031768-92031775	HepG2	liver:	n/a	n/a
29	CTCF	chr4:92034420-92034570	GM12865	blood:	n/a	chr4:92034457-92034478 chr4:92034455-92034473 chr4:92034456-92034472
30	CTCF	chr4:92034360-92034510	AG04449	skin:	n/a	chr4:92034457-92034478 chr4:92034455-92034473 chr4:92034456-92034472
31	CTCF	chr4:92038240-92038390	GM12867	blood:	n/a	n/a
32	CTCF	chr4:92014001-92014104	MCF-7	breast:	n/a	n/a
33	CTCF	chr4:92038100-92038250	MCF-7	breast:	n/a	chr4:92038207-92038228
34	CTCF	chr4:92034400-92034550	HL-60	blood:	n/a	chr4:92034457-92034478 chr4:92034455-92034473 chr4:92034456-92034472
35	CTCF	chr4:92013989-92014122	Gliobla	brain:	n/a	n/a
36	CTCF	chr4:92034323-92034603	Gliobla	brain:	n/a	chr4:92034457-92034478 chr4:92034455-92034473 chr4:92034456-92034472
37	CTCF	chr4:92038120-92038270	NHEK	skin:	n/a	chr4:92038207-92038228
38	CTCF	chr4:92013987-92014109	NHEK	skin:	n/a	n/a
39	CTCF	chr4:92013967-92014171	LNCaP	prostate:	n/a	n/a
40	CTCF	chr4:92034349-92034586	HepG2	liver:	n/a	chr4:92034457-92034478 chr4:92034455-92034473 chr4:92034456-92034472
41	CTCF	chr4:92034278-92034610	A549	lung:	n/a	chr4:92034457-92034478 chr4:92034455-92034473 chr4:92034456-92034472
42	CTCF	chr4:92013920-92014070	SAEC	small airway:	n/a	n/a
43	CTCF	chr4:92035520-92035670	HPAF	blood vessel:	n/a	n/a
44	CTCF	chr4:92038160-92038310	HCM	heart:	n/a	chr4:92038207-92038228
45	CTCF	chr4:92038160-92038310	HUVEC	blood vessel:	n/a	chr4:92038207-92038228
46	CTCF	chr4:92038142-92038271	HepG2	liver:	n/a	chr4:92038207-92038228
47	CTCF	chr4:92034320-92034470	HRE	kidney:	n/a	n/a
48	CTCF	chr4:92034400-92034550	GM12867	blood:	n/a	chr4:92034457-92034478 chr4:92034455-92034473 chr4:92034456-92034472
49	CTCF	chr4:92034333-92034649	H1-hESC	embryonic stem cell:	n/a	chr4:92034457-92034478 chr4:92034455-92034473 chr4:92034456-92034472
50	CTCF	chr4:92014053-92014141	Medullo	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:92008475-92008525	AG10803	skin:	n/a
2	chr4:92089238-92089288	HRCEpiC	kidney:	n/a
3	chr4:92089238-92089288	SKMC	muscle:	n/a
4	chr4:92048256-92048306	AoSMC	blood vessel:	n/a
5	chr4:92048256-92048306	BE2_C	brain:	n/a
6	chr4:92034737-92034787	BJ	skin:	n/a
7	chr4:92008475-92008525	GM19239	blood:	n/a
8	chr4:92048256-92048306	Jurkat	blood:	n/a
9	chr4:92048256-92048306	Caco-2	colon:	n/a
10	chr4:92048256-92048306	LNCaP	prostate:	n/a
11	chr4:92048256-92048306	HCM	heart:	n/a
12	chr4:92089238-92089288	AG10803	skin:	n/a
13	chr4:92008475-92008525	HL-60	blood:	n/a
14	chr4:92034737-92034787	GM19239	blood:	n/a
15	chr4:92034737-92034787	HL-60	blood:	n/a
16	chr4:92008475-92008525	BE2_C	brain:	n/a
17	chr4:92089238-92089288	T-47D	breast:	n/a
18	chr4:92089238-92089288	GM12878	blood:	n/a
19	chr4:92048256-92048306	NH-A	brain:	n/a
20	chr4:92034737-92034787	AG04449	skin:	fetal
21	chr4:92089238-92089288	HEEpiC	esophagus:	n/a
22	chr4:92008475-92008525	HCPEpiC	choroid plexus:	n/a
23	chr4:92034737-92034787	HUVEC	blood vessel:	n/a
24	chr4:92048256-92048306	MCF10A-Er-Src	breast:	n/a
25	chr4:92089238-92089288	HRPEpiC	eye:	n/a
26	chr4:92034737-92034787	PFSK-1	brain:	n/a
27	chr4:92008475-92008525	K562	blood:	n/a
28	chr4:92089238-92089288	HUVEC	blood vessel:	n/a
29	chr4:92008475-92008525	PFSK-1	brain:	n/a
30	chr4:92089238-92089288	SAEC	small airway:	n/a
31	chr4:92048256-92048306	AG10803	skin:	n/a
32	chr4:92034737-92034787	GM06990	blood:	n/a
33	chr4:92008475-92008525	GM06990	blood:	n/a
34	chr4:92089238-92089288	HL-60	blood:	n/a
35	chr4:92048256-92048306	HepG2	liver:	n/a
36	chr4:92089238-92089288	AG04450	lung:	fetal
37	chr4:92089238-92089288	NHDF-neo	bronchial:	n/a
38	chr4:92048256-92048306	HUVEC	blood vessel:	n/a
39	chr4:92048256-92048306	HRE	kidney:	n/a
40	chr4:92008475-92008525	NHBE	bronchial:	n/a
41	chr4:92048256-92048306	AG09319	gingival:	n/a
42	chr4:92034737-92034787	AG09309	skin:	n/a
43	chr4:92034737-92034787	HRPEpiC	eye:	n/a
44	chr4:92089238-92089288	Jurkat	blood:	n/a
45	chr4:92048256-92048306	GM19239	blood:	n/a
46	chr4:92034737-92034787	Hela-S3	cervix:	n/a
47	chr4:92034737-92034787	PrEC	prostate:	n/a
48	chr4:92089238-92089288	H1-hESC	embryonic stem cell:	embryo
49	chr4:92008475-92008525	HUVEC	blood vessel:	n/a
50	chr4:92089238-92089288	HCF	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:82295674..82298297-chr4:92009865..92012633,2	MCF-7	breast:
2	chr4:92034306..92035417-chr4:92423226..92424074,5	MCF-7	breast:
3	chr4:91982821..91984547-chr4:91990420..91991992,2	MCF-7	breast:
4	chr4:91971782..91973495-chr4:91983792..91985364,2	MCF-7	breast:
5	chr4:91982821..91984547-chr4:91990420..91991992,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-763F8.1.1-1	chr4:92029174-92029251	ENSG00000248984.1
2	lnc-RP11-763F8.1.1-1	chr4:92033750-92033941	ENSG00000248984.1

Variant related genes	Relation type
ENSG00000248984	TF binding region
ENSG00000248984	CpG island
ENSG00000178217	chromatin interactions
ENSG00000226659	chromatin interactions

Extended variants
information (count: 2675 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:2675 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10446698	chr4:91979094-91979095	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs549229066	chr4:91979157-91979158	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs571392261	chr4:91979177-91979178	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs368002125	chr4:91979182-91979183	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs569184545	chr4:91979219-91979220	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs138776887	chr4:91979243-91979244	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs13105567	chr4:91979273-91979274	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs188708307	chr4:91979362-91979363	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs192815772	chr4:91979380-91979381	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs72886652	chr4:91979410-91979411	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs554440690	chr4:91979424-91979425	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs28461191	chr4:91979439-91979440	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs534778194	chr4:91979443-91979444	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs10446699	chr4:91979460-91979461	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs550344675	chr4:91979467-91979468	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs185065095	chr4:91979475-91979476	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs140393045	chr4:91979479-91979480	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs371572219	chr4:91979504-91979505	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs564014789	chr4:91979507-91979508	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs145502640	chr4:91979520-91979521	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs13138447	chr4:91979540-91979541	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs368496732	chr4:91979568-91979569	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs189394511	chr4:91979603-91979604	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs529079772	chr4:91979659-91979660	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs549415422	chr4:91979695-91979696	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs563970196	chr4:91979764-91979765	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs78389444	chr4:91979767-91979768	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs141472043	chr4:91979782-91979783	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs551828641	chr4:91979831-91979832	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs180962968	chr4:91979882-91979883	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs576148615	chr4:91979910-91979911	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs571955015	chr4:91979914-91979915	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs534461870	chr4:91979943-91979944	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs150419430	chr4:91979959-91979960	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs567803522	chr4:91979982-91979983	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs536456595	chr4:91979989-91979990	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs554024667	chr4:91980069-91980070	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs71597223	chr4:91980079-91980080	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs57676449	chr4:91980081-91980082	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs537429887	chr4:91980082-91980083	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs557293641	chr4:91980121-91980122	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs370136900	chr4:91980122-91980123	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs9995159	chr4:91980149-91980150	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs115148963	chr4:91980160-91980161	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs532255952	chr4:91980214-91980215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs558168301	chr4:91980266-91980267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs566007958	chr4:91980299-91980300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs11288453	chr4:91980408-91980409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs138054596	chr4:91980411-91980412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs558606208	chr4:91980447-91980448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

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
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	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
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
primary effusion lymphomas	17116491	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Olfactory neuroblastoma	18408657	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	CNVD
Acute monocytic leukemia	16498392	CNVD
Multiple myeloma	16616336	CNVD
Esophageal adenocarcinoma	18820669	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myelofibrosis	22110671	CNVD
Parkinson disease	20877625	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Obesity	20622171	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	20164920	CNVD
Cancer	20164919	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Esophageal cancer	21851588	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:206 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:91972600-91985400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr4:91978400-91979600	Enhancers	HMEC	breast
3	chr4:91978600-91979600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr4:91978600-91980200	Enhancers	NHEK	skin
5	chr4:91978800-91984600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr4:91979000-91979600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr4:91979200-91979400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr4:91980200-91985400	Weak transcription	NHEK	skin
9	chr4:91980800-91981200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr4:91980800-91981400	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr4:91981000-91981400	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr4:91981200-91985200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr4:91981400-91985400	Weak transcription	HUES48 Cell Line	embryonic stem cell
14	chr4:91981400-91985400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr4:91983400-91983600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr4:91984200-91986400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr4:91984600-91985400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr4:91984600-91985600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr4:91984600-91985600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr4:91985000-91986400	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr4:91985000-91986400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr4:91985000-91986400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
23	chr4:91985000-91986400	Enhancers	Fetal Lung	lung
24	chr4:91985200-91985400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr4:91985200-91985600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr4:91985200-91985800	Enhancers	Rectal Smooth Muscle	rectum
27	chr4:91985200-91986000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr4:91985200-91986000	Enhancers	Adipose Nuclei	Adipose
29	chr4:91985200-91986000	Enhancers	Colon Smooth Muscle	Colon
30	chr4:91985200-91986000	Enhancers	Fetal Intestine Large	intestine
31	chr4:91985200-91986000	Enhancers	Hela-S3	cervix
32	chr4:91985200-91986200	Enhancers	Fetal Kidney	kidney
33	chr4:91985200-91986400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr4:91985200-91986400	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr4:91985200-91986400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr4:91985200-91987800	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr4:91985400-91985600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr4:91985400-91985800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr4:91985400-91985800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr4:91985400-91985800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr4:91985400-91985800	Enhancers	Brain Anterior Caudate	brain
42	chr4:91985400-91985800	Enhancers	Duodenum Smooth Muscle	Duodenum
43	chr4:91985400-91985800	Enhancers	Gastric	stomach
44	chr4:91985400-91986000	Enhancers	H1 Cell Line	embryonic stem cell
45	chr4:91985400-91986000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr4:91985400-91986000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr4:91985400-91986000	Enhancers	Aorta	Aorta
48	chr4:91985400-91986000	Enhancers	Fetal Intestine Small	intestine
49	chr4:91985400-91986000	Enhancers	Fetal Muscle Leg	muscle
50	chr4:91985400-91986000	Enhancers	Fetal Stomach	stomach

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