Variant report

Variant	nsv1049494
Chromosome Location	chr11:120400115-120453381
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	chr11:120402940-120403282	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:120411424-120411667	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:120418407-120419040	HepG2	liver:	n/a	chr11:120418419-120418435 chr11:120418420-120418436
4	ATF1	chr11:120401891-120401937	K562	blood:	n/a	n/a
5	ATF2	chr11:120450324-120450621	GM12878	blood:	n/a	n/a
6	ATF2	chr11:120435561-120436020	GM12878	blood:	n/a	n/a
7	ATF2	chr11:120435483-120436042	GM12878	blood:	n/a	n/a
8	ATF3	chr11:120403613-120403872	HepG2	liver:	n/a	n/a
9	BACH1	chr11:120425920-120426157	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr11:120434444-120434891	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr11:120435379-120435956	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr11:120445687-120445886	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr11:120435680-120435980	GM12878	blood:	n/a	n/a
14	BATF	chr11:120436002-120436451	GM12878	blood:	n/a	n/a
15	BATF	chr11:120435401-120435654	GM12878	blood:	n/a	n/a
16	BCL11A	chr11:120435579-120435979	GM12878	blood:	n/a	chr11:120435673-120435686 chr11:120435902-120435915 chr11:120435611-120435619
17	BCL11A	chr11:120435365-120436057	GM12878	blood:	n/a	chr11:120435418-120435431 chr11:120435450-120435459 chr11:120435377-120435390 chr11:120435673-120435686 chr11:120435375-120435388 chr11:120435420-120435429 chr11:120435902-120435915 chr11:120435421-120435434 chr11:120435611-120435619
18	BCL11A	chr11:120435295-120435536	GM12878	blood:	n/a	chr11:120435418-120435431 chr11:120435450-120435459 chr11:120435377-120435390 chr11:120435375-120435388 chr11:120435420-120435429 chr11:120435421-120435434
19	BCL3	chr11:120435444-120436021	GM12878	blood:	n/a	chr11:120435450-120435459 chr11:120435673-120435686 chr11:120435902-120435915 chr11:120435611-120435619
20	BCLAF1	chr11:120435338-120436027	GM12878	blood:	n/a	chr11:120435418-120435431 chr11:120435450-120435459 chr11:120435377-120435390 chr11:120435673-120435686 chr11:120435375-120435388 chr11:120435420-120435429 chr11:120435902-120435915 chr11:120435421-120435434 chr11:120435611-120435619
21	BCLAF1	chr11:120435624-120436097	GM12878	blood:	n/a	chr11:120435673-120435686 chr11:120435902-120435915
22	BHLHE40	chr11:120435438-120436096	GM12878	blood:	n/a	chr11:120435448-120435464 chr11:120435671-120435687
23	BHLHE40	chr11:120403540-120403913	HepG2	liver:	n/a	n/a
24	BHLHE40	chr11:120450423-120450709	GM12878	blood:	n/a	n/a
25	BHLHE40	chr11:120418584-120419105	HepG2	liver:	n/a	n/a
26	BRCA1	chr11:120435473-120435932	GM12878	blood:	n/a	n/a
27	BRCA1	chr11:120425812-120426076	H1-hESC	embryonic stem cell:	n/a	n/a
28	BRCA1	chr11:120417420-120417620	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr11:120403539-120403902	HepG2	liver:	n/a	chr11:120403717-120403728
30	CEBPB	chr11:120403474-120403849	HepG2	liver:	n/a	chr11:120403717-120403728
31	CEBPB	chr11:120403630-120403875	K562	blood:	n/a	chr11:120403717-120403728
32	CEBPB	chr11:120418618-120419260	IMR90	lung:	n/a	chr11:120419067-120419078
33	CEBPB	chr11:120434867-120434971	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr11:120439374-120439603	HepG2	liver:	n/a	chr11:120439448-120439459
35	CEBPB	chr11:120400749-120400897	HepG2	liver:	n/a	n/a
36	CEBPB	chr11:120432848-120433190	IMR90	lung:	n/a	chr11:120433015-120433026 chr11:120433016-120433027
37	CEBPB	chr11:120403548-120403868	A549	lung:	n/a	chr11:120403717-120403728
38	CEBPB	chr11:120432877-120433152	A549	lung:	n/a	chr11:120433015-120433026 chr11:120433016-120433027
39	CEBPB	chr11:120418648-120419049	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr11:120452125-120452351	Hela-S3	cervix:	n/a	chr11:120452198-120452209
41	CEBPB	chr11:120435711-120436099	IMR90	lung:	n/a	n/a
42	CEBPB	chr11:120400575-120401011	MCF-7	breast:	n/a	n/a
43	CEBPB	chr11:120441526-120441694	K562	blood:	n/a	chr11:120441603-120441614
44	CEBPB	chr11:120403532-120403915	HepG2	liver:	n/a	chr11:120403717-120403728
45	CEBPB	chr11:120452032-120452385	IMR90	lung:	n/a	chr11:120452198-120452209
46	CEBPB	chr11:120417327-120417732	IMR90	lung:	n/a	n/a
47	CEBPB	chr11:120439300-120439567	IMR90	lung:	n/a	chr11:120439448-120439459
48	CEBPB	chr11:120439205-120440009	HCT-116	colon:	n/a	chr11:120439448-120439459
49	CEBPB	chr11:120443435-120443751	HepG2	liver:	n/a	chr11:120443591-120443602 chr11:120443592-120443603
50	CEBPB	chr11:120402872-120403221	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:120435056-120435106	Hepatocyte	liver:	n/a
2	chr11:120435978-120436028	HL-60	blood:	n/a
3	chr11:120433356-120433406	PFSK-1	brain:	n/a
4	chr11:120440821-120440871	HepG2	liver:	n/a
5	chr11:120418900-120418950	NB4	blood:	n/a
6	chr11:120435056-120435106	Hepatocyte	liver:	n/a
7	chr11:120435978-120436028	HL-60	blood:	n/a
8	chr11:120433356-120433406	PFSK-1	brain:	n/a
9	chr11:120440821-120440871	HepG2	liver:	n/a
10	chr11:120418900-120418950	NB4	blood:	n/a
11	chr11:120435560-120435610	HepG2	liver:	n/a
12	chr11:120407665-120407715	HepG2	liver:	n/a
13	chr11:120426508-120426558	AG10803	skin:	n/a
14	chr11:120403285-120403335	NH-A	brain:	n/a
15	chr11:120417671-120417721	HIPEpiC	eye:	n/a
16	chr11:120426508-120426558	Hepatocyte	liver:	n/a
17	chr11:120420147-120420197	RPTEC	kidney:	n/a
18	chr11:120433996-120434046	AG10803	skin:	n/a
19	chr11:120435560-120435610	GM19239	blood:	n/a
20	chr11:120411816-120411866	HEEpiC	esophagus:	n/a
21	chr11:120435560-120435610	HRCEpiC	kidney:	n/a
22	chr11:120433032-120433082	ECC-1	luminal epithelium:	n/a
23	chr11:120439522-120439572	PFSK-1	brain:	n/a
24	chr11:120426508-120426558	T-47D	breast:	n/a
25	chr11:120435978-120436028	MCF10A-Er-Src	breast:	n/a
26	chr11:120433032-120433082	NB4	blood:	n/a
27	chr11:120403285-120403335	AG09309	skin:	n/a
28	chr11:120433356-120433406	GM12891	blood:	n/a
29	chr11:120418900-120418950	K562	blood:	n/a
30	chr11:120439522-120439572	MCF-7	breast:	n/a
31	chr11:120434880-120434930	HCPEpiC	choroid plexus:	n/a
32	chr11:120434979-120435029	ProgFib	skin:	n/a
33	chr11:120440821-120440871	HCF	heart:	n/a
34	chr11:120439522-120439572	HCF	heart:	n/a
35	chr11:120420147-120420197	HRPEpiC	eye:	n/a
36	chr11:120435915-120435965	LNCaP	prostate:	n/a
37	chr11:120440821-120440871	T-47D	breast:	n/a
38	chr11:120407665-120407715	H1-hESC	embryonic stem cell:	embryo
39	chr11:120435915-120435965	BE2_C	brain:	n/a
40	chr11:120434710-120434760	SKMC	muscle:	n/a
41	chr11:120403285-120403335	HL-60	blood:	n/a
42	chr11:120407665-120407715	HRCEpiC	kidney:	n/a
43	chr11:120435560-120435610	Caco-2	colon:	n/a
44	chr11:120440821-120440871	U87	brain:	n/a
45	chr11:120426508-120426558	Caco-2	colon:	n/a
46	chr11:120420147-120420197	SAEC	small airway:	n/a
47	chr11:120420147-120420197	GM12878	blood:	n/a
48	chr11:120407665-120407715	NHBE	bronchial:	n/a
49	chr11:120420147-120420197	NH-A	brain:	n/a
50	chr11:120434710-120434760	GM19239	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:120381768..120382394-chr11:120418781..120419873,3	MCF-7	breast:
2	chr11:120416706..120419405-chr11:120427869..120430423,2	K562	blood:
3	chr10:95029640..95030140-chr11:120440465..120441052,2	MCF-7	breast:
4	chr11:120400831..120403773-chr11:120408317..120411578,3	K562	blood:
5	chr11:120392853..120394571-chr11:120399376..120402273,2	MCF-7	breast:
6	chr11:120400831..120403773-chr11:120408682..120411578,3	K562	blood:
7	chr11:120415952..120418206-chr11:120428187..120430423,2	K562	blood:
8	chr11:120444035..120445726-chr11:120447574..120449245,2	K562	blood:
9	chr11:120433729..120435312-chr11:120435660..120438456,2	K562	blood:
10	chr11:120400831..120403773-chr11:120408682..120411578,3	K562	blood:
11	chr11:120415952..120418206-chr11:120428187..120430423,2	K562	blood:
12	chr11:120395943..120398129-chr11:120408243..120411100,2	K562	blood:
13	chr11:120416706..120419405-chr11:120427869..120430423,2	K562	blood:
14	chr11:120400831..120403773-chr11:120408317..120411578,3	K562	blood:
15	chr11:120444035..120445726-chr11:120447574..120449245,2	K562	blood:
16	chr11:120439418..120443663-chr11:120444829..120446935,3	K562	blood:

Variant related genes	Relation type
GRIK4	TF binding region
GRIK4	CpG island
ENSG00000149403	chromatin interactions

Extended variants
information (count: 2001 )
Associated
traits (count: 111 )

Variant overlapped rSNPs/rCNVs (count:2001 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2252359	chr11:120400149-120400150	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs188351142	chr11:120400163-120400164	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs115378293	chr11:120400214-120400215	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs191798083	chr11:120400260-120400261	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs117692796	chr11:120400283-120400284	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs552992486	chr11:120400294-120400295	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs571261532	chr11:120400306-120400307	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs538776825	chr11:120400311-120400312	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs116804506	chr11:120400317-120400318	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs142135412	chr11:120400329-120400330	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs114532992	chr11:120400333-120400334	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs555376207	chr11:120400357-120400358	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs58984886	chr11:120400380-120400381	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs527490340	chr11:120400404-120400405	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs573940893	chr11:120400411-120400412	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs2252222	chr11:120400419-120400420	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs373606907	chr11:120400473-120400474	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs61641913	chr11:120400488-120400489	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs532933460	chr11:120400517-120400518	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs545157077	chr11:120400518-120400519	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs145926303	chr11:120400520-120400521	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs57564610	chr11:120400551-120400552	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs374494786	chr11:120400561-120400562	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs183940756	chr11:120400568-120400569	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs189105443	chr11:120400569-120400570	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs181552071	chr11:120400579-120400580	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs532555440	chr11:120400592-120400593	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs57720932	chr11:120400632-120400633	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs185706036	chr11:120400668-120400669	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs571343261	chr11:120400669-120400670	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs538615793	chr11:120400714-120400715	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs563938621	chr11:120400715-120400716	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs544573578	chr11:120400719-120400720	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs138958858	chr11:120400753-120400754	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs569286313	chr11:120400759-120400760	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs190242176	chr11:120400764-120400765	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs367914477	chr11:120400835-120400836	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs60323374	chr11:120400892-120400893	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs541363053	chr11:120400893-120400894	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs78686911	chr11:120400935-120400936	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs374822272	chr11:120400970-120400971	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs577726442	chr11:120400991-120400992	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs180982567	chr11:120400994-120400995	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs563250567	chr11:120400995-120400996	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs529244719	chr11:120401003-120401004	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs7117380	chr11:120401070-120401071	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs542357990	chr11:120401095-120401096	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs561558224	chr11:120401136-120401137	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs528646888	chr11:120401161-120401162	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs139195006	chr11:120401198-120401199	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:111)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	20729466	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Cancer	22429812	CNVD
Breast cancer	16608533	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17603634	CNVD
Breast cancer	21364760	CNVD
Mental retardation	19966786	CNVD
Non-small cell lung cancer	21829676	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Ovarian cancer	21720365	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Neuroblastoma	17327916	CNVD
Malignant melanoma	17260012	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Renal cell carcinoma	21668985	CNVD
Developmental delay	21147756	CNVD
Emanuel syndrome	21549014	CNVD
Emanuel syndrome	18184694	CNVD
Non-syndromic sensorineural hearing loss	18184694	CNVD
Acute lymphoblastic leukemia	22581003	CNVD
Ovarian neoplasms	16753589	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cancer	21183584	CNVD
Retinoblastoma	22278416	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-syndromic sensorineural hearing loss	16829213	CNVD
Non-syndromic sensorineural hearing loss	16760666	CNVD
Squamous cell cancer	20885788	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Neurocytoma	17123091	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Central neurocytomas	17123091	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Hepatocellular carcinoma	16750200	CNVD
Multiple myeloma	17550852	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Acute myeloid leukemia	19651601	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	20409316	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Heart disease	20551144	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Autism	22543975	CNVD
Breast cancer	21509527	CNVD
Barrett''s syndrome	19417022	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:1159 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:120388800-120403400	Weak transcription	Right Atrium	heart
2	chr11:120398400-120402800	Weak transcription	Brain Cingulate Gyrus	brain
3	chr11:120398400-120403000	Weak transcription	NH-A	brain
4	chr11:120398600-120402000	Weak transcription	Ovary	ovary
5	chr11:120398600-120402800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr11:120398600-120403000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr11:120398600-120403000	Weak transcription	HUES64 Cell Line	embryonic stem cell
8	chr11:120398600-120403200	Weak transcription	HUES48 Cell Line	embryonic stem cell
9	chr11:120398600-120403200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
10	chr11:120398600-120403400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr11:120398600-120403400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr11:120398600-120417200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr11:120398800-120402800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr11:120398800-120408800	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr11:120399000-120402800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr11:120400000-120402600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr11:120400000-120404200	Enhancers	Fetal Intestine Large	intestine
18	chr11:120400000-120404400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
19	chr11:120400400-120401600	Enhancers	Fetal Intestine Small	intestine
20	chr11:120401600-120402600	Weak transcription	Fetal Intestine Small	intestine
21	chr11:120401600-120402600	Bivalent Enhancer	HepG2	liver
22	chr11:120402000-120403200	Enhancers	Ovary	ovary
23	chr11:120402600-120402800	Flanking Bivalent TSS/Enh	HepG2	liver
24	chr11:120402600-120403200	Enhancers	Cortex derived primary cultured neurospheres	brain
25	chr11:120402600-120404000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr11:120402600-120404400	Enhancers	Fetal Intestine Small	intestine
27	chr11:120402800-120403000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
28	chr11:120402800-120403000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr11:120402800-120403000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr11:120402800-120403000	Enhancers	Spleen	Spleen
31	chr11:120402800-120403000	Bivalent Enhancer	Osteobl	bone
32	chr11:120402800-120403200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr11:120402800-120403200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr11:120402800-120403200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
35	chr11:120402800-120403600	Flanking Active TSS	NHDF-Ad	bronchial
36	chr11:120402800-120403800	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr11:120402800-120403800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr11:120402800-120403800	Enhancers	Brain Cingulate Gyrus	brain
39	chr11:120402800-120403800	Enhancers	Brain Hippocampus Middle	brain
40	chr11:120402800-120403800	Enhancers	Fetal Muscle Leg	muscle
41	chr11:120402800-120403800	Enhancers	Placenta	Placenta
42	chr11:120402800-120404000	Flanking Active TSS	HepG2	liver
43	chr11:120402800-120404200	Enhancers	Breast Myoepithelial Primary Cells	Breast
44	chr11:120403000-120403200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr11:120403000-120403200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr11:120403000-120403200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr11:120403000-120403200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr11:120403000-120403200	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr11:120403000-120403200	Enhancers	Fetal Lung	lung
50	chr11:120403000-120403200	Bivalent Enhancer	Fetal Stomach	stomach

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