Variant report

Variant	esv2759267
Chromosome Location	chr4:91946664-92146114
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	chr4:91983060-91983121	K562	blood:	n/a	n/a
3	BACH1	chr4:92007259-92007496	H1-hESC	embryonic stem cell:	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	BHLHE40	chr4:92128792-92128991	GM12878	blood:	n/a	n/a
7	BRCA1	chr4:91985692-91985806	H1-hESC	embryonic stem cell:	n/a	n/a
8	CBX3	chr4:92024996-92025295	K562	blood:	n/a	n/a
9	CEBPB	chr4:92063832-92063977	H1-hESC	embryonic stem cell:	n/a	chr4:92063859-92063870
10	CEBPB	chr4:92063721-92064028	IMR90	lung:	n/a	chr4:92063859-92063870
11	CEBPB	chr4:92061834-92062206	HepG2	liver:	n/a	chr4:92062016-92062027
12	CEBPB	chr4:92061857-92062184	IMR90	lung:	n/a	chr4:92062016-92062027
13	CEBPB	chr4:92044617-92044895	A549	lung:	n/a	chr4:92044758-92044769 chr4:92044718-92044729
14	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
15	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
16	CEBPB	chr4:92063745-92063988	A549	lung:	n/a	chr4:92063859-92063870
17	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
18	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
19	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
20	CEBPB	chr4:92044571-92044854	HepG2	liver:	n/a	chr4:92044758-92044769 chr4:92044718-92044729
21	CEBPB	chr4:92061856-92062186	A549	lung:	n/a	chr4:92062016-92062027
22	CEBPB	chr4:92061869-92062156	K562	blood:	n/a	chr4:92062016-92062027
23	CEBPB	chr4:92063703-92064031	HepG2	liver:	n/a	chr4:92063859-92063870
24	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
25	CEBPB	chr4:91974973-91975287	HepG2	liver:	n/a	chr4:91975130-91975141
26	CEBPB	chr4:92044637-92044818	H1-hESC	embryonic stem cell:	n/a	chr4:92044758-92044769 chr4:92044718-92044729
27	CEBPB	chr4:92007232-92007488	H1-hESC	embryonic stem cell:	n/a	n/a
28	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
29	CEBPB	chr4:92034320-92034601	ECC-1	luminal epithelium:	n/a	n/a
30	CEBPZ	chr4:92031768-92031775	HepG2	liver:	n/a	n/a
31	CHD1	chr4:92143874-92143897	H1-hESC	embryonic stem cell:	n/a	n/a
32	CREB1	chr4:91946453-91946857	H1-hESC	embryonic stem cell:	n/a	n/a
33	CREB1	chr4:91946512-91946765	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr4:92034335-92034569	LNCaP	prostate:	n/a	chr4:92034457-92034478 chr4:92034455-92034473 chr4:92034456-92034472
35	CTCF	chr4:92034360-92034510	GM12867	blood:	n/a	chr4:92034457-92034478 chr4:92034455-92034473 chr4:92034456-92034472
36	CTCF	chr4:92038140-92038290	HPAF	blood vessel:	n/a	chr4:92038207-92038228
37	CTCF	chr4:92034380-92034530	HEK293	kidney:	n/a	chr4:92034457-92034478 chr4:92034455-92034473 chr4:92034456-92034472
38	CTCF	chr4:92038062-92038380	IMR90	lung:	n/a	chr4:92038207-92038228
39	CTCF	chr4:92034331-92034567	GM10248	blood:	n/a	chr4:92034457-92034478 chr4:92034455-92034473 chr4:92034456-92034472
40	CTCF	chr4:92034400-92034550	HUVEC	blood vessel:	n/a	chr4:92034457-92034478 chr4:92034455-92034473 chr4:92034456-92034472
41	CTCF	chr4:92034369-92034524	NHEK	skin:	n/a	chr4:92034457-92034478 chr4:92034455-92034473 chr4:92034456-92034472
42	CTCF	chr4:92034080-92034230	GM12872	blood:	n/a	n/a
43	CTCF	chr4:92034400-92034550	GM12875	blood:	n/a	chr4:92034457-92034478 chr4:92034455-92034473 chr4:92034456-92034472
44	CTCF	chr4:92013940-92014090	RPTEC	kidney:	n/a	n/a
45	CTCF	chr4:92034357-92034570	HepG2	liver:	n/a	chr4:92034457-92034478 chr4:92034455-92034473 chr4:92034456-92034472
46	CTCF	chr4:92034360-92034510	GM12873	blood:	n/a	chr4:92034457-92034478 chr4:92034455-92034473 chr4:92034456-92034472
47	CTCF	chr4:92038153-92038336	GM13977	blood:	n/a	chr4:92038207-92038228
48	CTCF	chr4:92038120-92038270	HBMEC	blood vessel:	n/a	chr4:92038207-92038228
49	CTCF	chr4:92034360-92034510	HVMF	connective:	n/a	chr4:92034457-92034478 chr4:92034455-92034473 chr4:92034456-92034472
50	CTCF	chr4:92034336-92034572	A549	lung:	n/a	chr4:92034457-92034478 chr4:92034455-92034473 chr4:92034456-92034472

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:92048256-92048306	PANC-1	pancreas:	n/a
2	chr4:92008475-92008525	SKMC	muscle:	n/a
3	chr4:92048256-92048306	PANC-1	pancreas:	n/a
4	chr4:92008475-92008525	SKMC	muscle:	n/a
5	chr4:92089238-92089288	HRCEpiC	kidney:	n/a
6	chr4:92089238-92089288	HEEpiC	esophagus:	n/a
7	chr4:92048256-92048306	HUVEC	blood vessel:	n/a
8	chr4:92089238-92089288	AG04449	skin:	fetal
9	chr4:92089238-92089288	T-47D	breast:	n/a
10	chr4:92089238-92089288	AoSMC	blood vessel:	n/a
11	chr4:92034737-92034787	SK-N-MC	brain:	n/a
12	chr4:92089238-92089288	NH-A	brain:	n/a
13	chr4:92008475-92008525	GM19239	blood:	n/a
14	chr4:92008475-92008525	HRCEpiC	kidney:	n/a
15	chr4:92048256-92048306	SK-N-SH	brain:	n/a
16	chr4:92008475-92008525	PANC-1	pancreas:	n/a
17	chr4:92008475-92008525	HRE	kidney:	n/a
18	chr4:92008475-92008525	CMK	blood:	n/a
19	chr4:92034737-92034787	HCPEpiC	choroid plexus:	n/a
20	chr4:92089238-92089288	HMEC	breast:	n/a
21	chr4:92048256-92048306	AG09309	skin:	n/a
22	chr4:92089238-92089288	AG09319	gingival:	n/a
23	chr4:92008475-92008525	U87	brain:	n/a
24	chr4:92008475-92008525	GM12878	blood:	n/a
25	chr4:92034737-92034787	AG04450	lung:	fetal
26	chr4:92048256-92048306	GM12891	blood:	n/a
27	chr4:92089238-92089288	GM19239	blood:	n/a
28	chr4:92048256-92048306	T-47D	breast:	n/a
29	chr4:92034737-92034787	SK-N-SH	brain:	n/a
30	chr4:92008475-92008525	HCF	heart:	n/a
31	chr4:92089238-92089288	HCM	heart:	n/a
32	chr4:92089238-92089288	RPTEC	kidney:	n/a
33	chr4:92089238-92089288	U87	brain:	n/a
34	chr4:92089238-92089288	BJ	skin:	n/a
35	chr4:92089238-92089288	MCF10A-Er-Src	breast:	n/a
36	chr4:92034737-92034787	PANC-1	pancreas:	n/a
37	chr4:92089238-92089288	HAEpiC	amniotic membrane:	n/a
38	chr4:92008475-92008525	ProgFib	skin:	n/a
39	chr4:92034737-92034787	HAEpiC	amniotic membrane:	n/a
40	chr4:92089238-92089288	HL-60	blood:	n/a
41	chr4:92034737-92034787	AG10803	skin:	n/a
42	chr4:92089238-92089288	K562	blood:	n/a
43	chr4:92034737-92034787	HEK293	kidney:	embryo
44	chr4:92034737-92034787	HPAEpiC	pulmonary alveolar:	n/a
45	chr4:92034737-92034787	Hepatocyte	liver:	n/a
46	chr4:92089238-92089288	A549	lung:	n/a
47	chr4:92048256-92048306	GM12878	blood:	n/a
48	chr4:92048256-92048306	NH-A	brain:	n/a
49	chr4:92048256-92048306	GM12892	blood:	n/a
50	chr4:92048256-92048306	ovcar-3	ovarian:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:82295674..82298297-chr4:92009865..92012633,2	MCF-7	breast:
2	chr4:91982821..91984547-chr4:91990420..91991992,2	MCF-7	breast:
3	chr4:91971782..91973495-chr4:91983792..91985364,2	MCF-7	breast:
4	chr4:91871450..91872421-chr4:91953829..91954477,2	MCF-7	breast:
5	chr4:92118886..92121028-chr6:31337898..31340855,2	MCF-7	breast:
6	chr4:91971782..91973495-chr4:91983792..91985364,2	MCF-7	breast:
7	chr4:91903199..91905652-chr4:91956772..91959683,2	MCF-7	breast:
8	chr4:92034306..92035417-chr4:92423226..92424074,5	MCF-7	breast:
9	chr4:91982821..91984547-chr4:91990420..91991992,2	MCF-7	breast:

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

Variant related genes	Relation type
ENSG00000248984	TF binding region
ENSG00000248984	CpG island
ENSG00000201658	chromatin interactions
ENSG00000226659	chromatin interactions
ENSG00000178217	chromatin interactions

Extended variants
information (count: 4156 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:4156 , 50 per page) page: 1 2 3 4 5 6 7 ... 84

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs540051374	chr4:91946705-91946706	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs566964431	chr4:91946750-91946751	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs371547256	chr4:91946782-91946783	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs10030101	chr4:91946794-91946795	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs556002241	chr4:91946808-91946809	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs562940664	chr4:91946814-91946815	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs556676653	chr4:91946887-91946888	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs201884598	chr4:91946895-91946896	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs574793210	chr4:91946913-91946914	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs139900249	chr4:91946934-91946935	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs12504169	chr4:91946944-91946945	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs527859116	chr4:91946981-91946982	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs185942643	chr4:91946985-91946986	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs190356017	chr4:91947007-91947008	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs57040256	chr4:91947008-91947009	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs375207802	chr4:91947013-91947014	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs140770701	chr4:91947072-91947073	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs201779194	chr4:91947073-91947074	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs149413883	chr4:91947095-91947096	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs548701060	chr4:91947156-91947157	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs568865013	chr4:91947224-91947225	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs537732406	chr4:91947397-91947398	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs146358814	chr4:91947506-91947507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs577878762	chr4:91947516-91947517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs182419504	chr4:91947531-91947532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs553560512	chr4:91947532-91947533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs573785736	chr4:91947607-91947608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs542758324	chr4:91947689-91947690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs186983387	chr4:91947690-91947691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs191211378	chr4:91947705-91947706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs182536089	chr4:91947762-91947763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs73834725	chr4:91947776-91947777	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs565526800	chr4:91947800-91947801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs528000888	chr4:91947815-91947816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs72667522	chr4:91947828-91947829	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs72667524	chr4:91947871-91947872	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs185828549	chr4:91947873-91947874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs190155831	chr4:91947984-91947985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs200894871	chr4:91947998-91947999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs528836369	chr4:91954103-91954104	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs10856881	chr4:91954105-91954106	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs193062886	chr4:91954123-91954124	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs561147100	chr4:91954181-91954182	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs142784918	chr4:91954210-91954211	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs377472989	chr4:91954221-91954222	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs183105926	chr4:91954246-91954247	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs537792304	chr4:91954267-91954268	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs576351109	chr4:91954308-91954309	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs373631943	chr4:91954392-91954393	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs543582144	chr4:91954444-91954445	Enhancers	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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Esophageal cancer	21851588	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:300 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:91941800-91948000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr4:91946600-91947400	Enhancers	H1 Cell Line	embryonic stem cell
3	chr4:91946600-91947400	Enhancers	Fetal Lung	lung
4	chr4:91947000-91947400	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr4:91954000-91954600	Enhancers	Pancreas	Pancrea
6	chr4:91954600-91958400	Weak transcription	Pancreas	Pancrea
7	chr4:91956400-91957200	Enhancers	Colon Smooth Muscle	Colon
8	chr4:91957200-91958400	Weak transcription	Colon Smooth Muscle	Colon
9	chr4:91958400-91958600	Enhancers	Colon Smooth Muscle	Colon
10	chr4:91958400-91958600	Enhancers	Pancreas	Pancrea
11	chr4:91961600-91961800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr4:91961600-91962000	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr4:91961600-91962000	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr4:91961600-91962400	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr4:91961800-91962000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr4:91972600-91985400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr4:91977800-91978000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr4:91978000-91978600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr4:91978400-91979600	Enhancers	HMEC	breast
20	chr4:91978600-91978800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr4:91978600-91979600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr4:91978600-91980200	Enhancers	NHEK	skin
23	chr4:91978800-91984600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr4:91979000-91979600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr4:91979200-91979400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr4:91980200-91985400	Weak transcription	NHEK	skin
27	chr4:91980800-91981200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr4:91980800-91981400	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr4:91981000-91981400	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr4:91981200-91985200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr4:91981400-91985400	Weak transcription	HUES48 Cell Line	embryonic stem cell
32	chr4:91981400-91985400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
33	chr4:91983400-91983600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr4:91984200-91986400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr4:91984600-91985400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr4:91984600-91985600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr4:91984600-91985600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr4:91985000-91986400	Enhancers	Cortex derived primary cultured neurospheres	brain
39	chr4:91985000-91986400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr4:91985000-91986400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
41	chr4:91985000-91986400	Enhancers	Fetal Lung	lung
42	chr4:91985200-91985400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr4:91985200-91985600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr4:91985200-91985800	Enhancers	Rectal Smooth Muscle	rectum
45	chr4:91985200-91986000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr4:91985200-91986000	Enhancers	Adipose Nuclei	Adipose
47	chr4:91985200-91986000	Enhancers	Colon Smooth Muscle	Colon
48	chr4:91985200-91986000	Enhancers	Fetal Intestine Large	intestine
49	chr4:91985200-91986000	Enhancers	Hela-S3	cervix
50	chr4:91985200-91986200	Enhancers	Fetal Kidney	kidney

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