Variant report

Variant	nsv522474
Chromosome Location	chr11:121356968-121436270
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:779)
CpG islands
(count:305)
Chromatin interactive
region (count:20)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:779 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:121434568-121436352	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:121424261-121425076	HepG2	liver:	n/a	n/a
3	ATF2	chr11:121408334-121409302	GM12878	blood:	n/a	n/a
4	ATF2	chr11:121365047-121365911	GM12878	blood:	n/a	n/a
5	ATF2	chr11:121427667-121428670	GM12878	blood:	n/a	n/a
6	ATF2	chr11:121408632-121409321	GM12878	blood:	n/a	n/a
7	ATF2	chr11:121427646-121428865	GM12878	blood:	n/a	n/a
8	ATF2	chr11:121391957-121392746	GM12878	blood:	n/a	n/a
9	ATF2	chr11:121365396-121365790	GM12878	blood:	n/a	n/a
10	ATF2	chr11:121422143-121422626	GM12878	blood:	n/a	n/a
11	ATF2	chr11:121409737-121410222	GM12878	blood:	n/a	n/a
12	BATF	chr11:121428018-121428415	GM12878	blood:	n/a	n/a
13	BATF	chr11:121422179-121422460	GM12878	blood:	n/a	n/a
14	BATF	chr11:121428063-121428433	GM12878	blood:	n/a	n/a
15	BATF	chr11:121421038-121421339	GM12878	blood:	n/a	chr11:121421136-121421146 chr11:121421140-121421150 chr11:121421139-121421150
16	BATF	chr11:121392104-121392699	GM12878	blood:	n/a	chr11:121392366-121392377
17	BATF	chr11:121408678-121409192	GM12878	blood:	n/a	n/a
18	BATF	chr11:121408778-121409098	GM12878	blood:	n/a	n/a
19	BCL11A	chr11:121428003-121428407	GM12878	blood:	n/a	n/a
20	BCL11A	chr11:121408718-121409187	GM12878	blood:	n/a	n/a
21	BCL11A	chr11:121428012-121428485	GM12878	blood:	n/a	n/a
22	BCL3	chr11:121392250-121392653	GM12878	blood:	n/a	n/a
23	BCL3	chr11:121427895-121428498	GM12878	blood:	n/a	n/a
24	BCL3	chr11:121388224-121388763	GM12878	blood:	n/a	n/a
25	BCLAF1	chr11:121427794-121428671	GM12878	blood:	n/a	n/a
26	BCLAF1	chr11:121408673-121409236	GM12878	blood:	n/a	n/a
27	BHLHE40	chr11:121365441-121365812	GM12878	blood:	n/a	n/a
28	BHLHE40	chr11:121427958-121428527	GM12878	blood:	n/a	n/a
29	BHLHE40	chr11:121424172-121424952	HepG2	liver:	n/a	chr11:121424273-121424282 chr11:121424273-121424282 chr11:121424271-121424284 chr11:121424272-121424281 chr11:121424267-121424288
30	BHLHE40	chr11:121412653-121412721	GM12878	blood:	n/a	n/a
31	BHLHE40	chr11:121431972-121432209	GM12878	blood:	n/a	n/a
32	BHLHE40	chr11:121408731-121409264	GM12878	blood:	n/a	n/a
33	BHLHE40	chr11:121424159-121424381	K562	blood:	n/a	chr11:121424273-121424282 chr11:121424273-121424282 chr11:121424271-121424284 chr11:121424272-121424281 chr11:121424267-121424288
34	BHLHE40	chr11:121392151-121392412	GM12878	blood:	n/a	n/a
35	BHLHE40	chr11:121422350-121422391	GM12878	blood:	n/a	n/a
36	CEBPB	chr11:121424496-121424975	HepG2	liver:	n/a	n/a
37	CEBPB	chr11:121427603-121427670	HepG2	liver:	n/a	n/a
38	CEBPB	chr11:121424534-121424786	HepG2	liver:	n/a	n/a
39	CEBPB	chr11:121385842-121385959	HepG2	liver:	n/a	chr11:121385905-121385916
40	CEBPB	chr11:121435293-121435424	HepG2	liver:	n/a	n/a
41	CEBPB	chr11:121360608-121360843	HepG2	liver:	n/a	chr11:121360722-121360733
42	CEBPB	chr11:121391081-121391362	HepG2	liver:	n/a	chr11:121391236-121391247
43	CEBPB	chr11:121391080-121391385	Hela-S3	cervix:	n/a	chr11:121391236-121391247
44	CEBPB	chr11:121435235-121436105	HepG2	liver:	n/a	n/a
45	CEBPB	chr11:121390445-121390617	IMR90	lung:	n/a	n/a
46	CEBPB	chr11:121435784-121436087	HepG2	liver:	n/a	n/a
47	CEBPB	chr11:121365269-121365928	GM12878	blood:	n/a	n/a
48	CEBPB	chr11:121373827-121374060	IMR90	lung:	n/a	n/a
49	CEBPB	chr11:121435239-121436202	HepG2	liver:	n/a	n/a
50	CEBPB	chr11:121435663-121436119	HepG2	liver:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:121370102-121370152	HCT-116	colon:	n/a
2	chr11:121421298-121421348	Hepatocyte	liver:	n/a
3	chr11:121421298-121421348	NHDF-neo	bronchial:	n/a
4	chr11:121421298-121421348	HAEpiC	amniotic membrane:	n/a
5	chr11:121421206-121421256	SK-N-SH	brain:	n/a
6	chr11:121370102-121370152	T-47D	breast:	n/a
7	chr11:121421298-121421348	SKMC	muscle:	n/a
8	chr11:121421206-121421256	AG10803	skin:	n/a
9	chr11:121422921-121422971	Caco-2	colon:	n/a
10	chr11:121378959-121379009	HRCEpiC	kidney:	n/a
11	chr11:121378959-121379009	NB4	blood:	n/a
12	chr11:121370102-121370152	HRCEpiC	kidney:	n/a
13	chr11:121378959-121379009	HMEC	breast:	n/a
14	chr11:121370102-121370152	MCF-7	breast:	n/a
15	chr11:121378959-121379009	HCF	heart:	n/a
16	chr11:121421206-121421256	AG09319	gingival:	n/a
17	chr11:121422921-121422971	ovcar-3	ovarian:	n/a
18	chr11:121421298-121421348	ProgFib	skin:	n/a
19	chr11:121378959-121379009	NH-A	brain:	n/a
20	chr11:121421298-121421348	BJ	skin:	n/a
21	chr11:121421206-121421256	GM12892	blood:	n/a
22	chr11:121422921-121422971	HCPEpiC	choroid plexus:	n/a
23	chr11:121370102-121370152	CMK	blood:	n/a
24	chr11:121378959-121379009	HRPEpiC	eye:	n/a
25	chr11:121421206-121421256	CMK	blood:	n/a
26	chr11:121422921-121422971	AG09309	skin:	n/a
27	chr11:121421206-121421256	HMEC	breast:	n/a
28	chr11:121370102-121370152	HCF	heart:	n/a
29	chr11:121422921-121422971	MCF10A-Er-Src	breast:	n/a
30	chr11:121370102-121370152	BE2_C	brain:	n/a
31	chr11:121421298-121421348	GM12891	blood:	n/a
32	chr11:121421298-121421348	HRCEpiC	kidney:	n/a
33	chr11:121378959-121379009	Jurkat	blood:	n/a
34	chr11:121421298-121421348	LNCaP	prostate:	n/a
35	chr11:121378959-121379009	AG04449	skin:	fetal
36	chr11:121421206-121421256	NT2-D1	testis:	n/a
37	chr11:121378959-121379009	GM06990	blood:	n/a
38	chr11:121421206-121421256	U87	brain:	n/a
39	chr11:121421298-121421348	SAEC	small airway:	n/a
40	chr11:121421298-121421348	PrEC	prostate:	n/a
41	chr11:121421298-121421348	HCPEpiC	choroid plexus:	n/a
42	chr11:121370102-121370152	Caco-2	colon:	n/a
43	chr11:121421298-121421348	GM19239	blood:	n/a
44	chr11:121421206-121421256	NH-A	brain:	n/a
45	chr11:121370102-121370152	ovcar-3	ovarian:	n/a
46	chr11:121422921-121422971	SK-N-MC	brain:	n/a
47	chr11:121421206-121421256	HEEpiC	esophagus:	n/a
48	chr11:121421298-121421348	AG09309	skin:	n/a
49	chr11:121378959-121379009	U87	brain:	n/a
50	chr11:121421206-121421256	RPTEC	kidney:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:121189964..121190649-chr11:121404609..121405478,2	MCF-7	breast:
2	chr11:121352073..121354474-chr11:121360345..121361966,2	MCF-7	breast:
3	chr11:121417486..121419268-chr11:121423006..121424690,2	K562	blood:
4	chr11:121376745..121379548-chr11:121384857..121386768,2	K562	blood:
5	chr11:121410810..121412961-chr11:121413789..121415504,2	K562	blood:
6	chr11:121394952..121397845-chr11:121402753..121405692,2	MCF-7	breast:
7	chr11:121417486..121419268-chr11:121423006..121424690,2	K562	blood:
8	chr11:121410810..121412961-chr11:121413789..121415504,2	K562	blood:
9	chr11:121421973..121423499-chr11:121425332..121427646,2	K562	blood:
10	chr11:121376745..121379548-chr11:121384857..121386768,2	K562	blood:
11	chr11:121358992..121360735-chr11:121362875..121365300,2	MCF-7	breast:
12	chr11:121317734..121318260-chr11:121404508..121405129,2	MCF-7	breast:
13	chr11:121191941..121192910-chr11:121404447..121405457,5	MCF-7	breast:
14	chr11:121358992..121360735-chr11:121362875..121365300,2	MCF-7	breast:
15	chr11:121394952..121397845-chr11:121402753..121405692,2	MCF-7	breast:
16	chr11:121405326..121406874-chr11:121420837..121422474,2	MCF-7	breast:
17	chr11:121322535..121323236-chr11:121404278..121405268,4	MCF-7	breast:
18	chr11:121417486..121419268-chr11:121422496..121424690,3	K562	blood:
19	chr11:121405326..121406874-chr11:121420837..121422474,2	MCF-7	breast:
20	chr11:121417486..121419268-chr11:121422496..121424690,3	K562	blood:

No data

Variant related genes	Relation type
SORL1	TF binding region
SORL1	CpG island
ENSG00000137642	chromatin interactions

Extended variants
information (count: 2996 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:2996 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11600875	chr11:121356968-121356969	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs113238791	chr11:121356975-121356976	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs546212932	chr11:121356997-121356998	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs577695309	chr11:121357006-121357007	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs189783286	chr11:121357072-121357073	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs576790521	chr11:121357077-121357078	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs544177211	chr11:121357088-121357089	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs562881657	chr11:121357113-121357114	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs551145449	chr11:121357190-121357191	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs181628689	chr11:121357193-121357194	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs79991092	chr11:121357207-121357208	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs184311181	chr11:121357211-121357212	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs542020891	chr11:121357212-121357213	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs374769170	chr11:121357220-121357221	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs545349849	chr11:121357228-121357229	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs527800420	chr11:121357243-121357244	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs189471750	chr11:121357250-121357251	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs138337950	chr11:121357252-121357253	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs531644113	chr11:121357255-121357256	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs550189735	chr11:121357313-121357314	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs569224604	chr11:121357314-121357315	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs536506998	chr11:121357361-121357362	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs11605510	chr11:121357364-121357365	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs566516501	chr11:121357378-121357379	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs533965680	chr11:121357382-121357383	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs558401773	chr11:121357390-121357391	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs576860033	chr11:121357409-121357410	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs543848165	chr11:121357423-121357424	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs555692875	chr11:121357429-121357430	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs112817319	chr11:121357435-121357436	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs373363655	chr11:121357480-121357481	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs542082067	chr11:121357484-121357485	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs560758912	chr11:121357488-121357489	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs181899256	chr11:121357511-121357512	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs546363198	chr11:121357533-121357534	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs370691409	chr11:121357579-121357580	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs146800913	chr11:121357583-121357584	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs186065023	chr11:121357595-121357596	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs12287560	chr11:121357620-121357621	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs145725562	chr11:121357657-121357658	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs548530143	chr11:121357725-121357726	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs528606017	chr11:121357746-121357747	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs140975241	chr11:121357750-121357751	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs190874936	chr11:121357752-121357753	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs579131	chr11:121357766-121357767	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs537507082	chr11:121357777-121357778	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs555754453	chr11:121357786-121357787	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs117635103	chr11:121357794-121357795	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs535061637	chr11:121357804-121357805	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs180745953	chr11:121357878-121357879	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Glioblastoma multiforme	21080181	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
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
Invasive pancreatic ductal carcinoma	16982739	CNVD
Ovarian cancer	21720365	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
Squamous cell cancer	20885788	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Hepatocellular carcinoma	16750200	CNVD
Multiple myeloma	17550852	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Heart disease	20551144	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Breast cancer	21509527	CNVD
Barrett''s syndrome	19417022	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	21385341	CNVD
Multiple myeloma	16461302	CNVD
Burkitt''s lymphoma	18698080	CNVD
Prostate cancer	23792589	CNVD
Effusion lymphoma	18079361	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Medulloblastoma	21163964	CNVD

Chromatin state (count:2427 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:121337400-121358800	Weak transcription	Right Ventricle	heart
2	chr11:121337600-121358800	Weak transcription	Brain Germinal Matrix	brain
3	chr11:121339000-121358200	Weak transcription	Aorta	Aorta
4	chr11:121344200-121358200	Weak transcription	Colon Smooth Muscle	Colon
5	chr11:121347800-121359400	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr11:121349800-121358200	Weak transcription	Rectal Smooth Muscle	rectum
7	chr11:121349800-121365000	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr11:121349800-121393000	Weak transcription	Colonic Mucosa	Colon
9	chr11:121350000-121357800	Weak transcription	Esophagus	oesophagus
10	chr11:121350000-121401400	Weak transcription	Fetal Brain Male	brain
11	chr11:121350200-121367800	Weak transcription	Fetal Kidney	kidney
12	chr11:121350400-121393200	Weak transcription	Gastric	stomach
13	chr11:121350600-121357600	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chr11:121350600-121359600	Weak transcription	Stomach Mucosa	stomach
15	chr11:121350800-121357600	Weak transcription	Fetal Brain Female	brain
16	chr11:121350800-121357600	Weak transcription	Stomach Smooth Muscle	stomach
17	chr11:121350800-121368400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr11:121351200-121366600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr11:121351400-121384600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
20	chr11:121352800-121377600	Strong transcription	HepG2	liver
21	chr11:121353200-121357400	Weak transcription	Fetal Stomach	stomach
22	chr11:121353200-121358200	Weak transcription	Brain Angular Gyrus	brain
23	chr11:121353400-121358000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
24	chr11:121353400-121358400	Weak transcription	HUES48 Cell Line	embryonic stem cell
25	chr11:121353600-121357000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
26	chr11:121353600-121357600	Weak transcription	Brain Anterior Caudate	brain
27	chr11:121353600-121357600	Weak transcription	Brain Inferior Temporal Lobe	brain
28	chr11:121353600-121357800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr11:121353600-121358200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
30	chr11:121353600-121358400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
31	chr11:121353600-121358400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr11:121353600-121358600	Weak transcription	Lung	lung
33	chr11:121353600-121364400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
34	chr11:121353600-121367200	Weak transcription	Fetal Lung	lung
35	chr11:121353600-121377000	Weak transcription	Pancreas	Pancrea
36	chr11:121353800-121358400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr11:121353800-121358600	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr11:121353800-121358600	Weak transcription	NHEK	skin
39	chr11:121353800-121359000	Genic enhancers	Primary T cells fromperipheralblood	blood
40	chr11:121353800-121365000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr11:121353800-121365000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr11:121353800-121374200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr11:121354200-121357600	Weak transcription	HUES6 Cell Line	embryonic stem cell
44	chr11:121354200-121357600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr11:121354200-121357800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr11:121354200-121359400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr11:121354200-121365000	Weak transcription	HMEC	breast
48	chr11:121354400-121357200	Genic enhancers	Primary T helper memory cells from peripheral blood 2	blood
49	chr11:121354400-121364000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
50	chr11:121354400-121364600	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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