Variant report

Variant	nsv523356
Chromosome Location	chr11:33777334-33797408
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:479)
CpG islands
(count:859)
Chromatin interactive
region (count:24)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:479 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:33784242-33784384	K562	blood:	n/a	n/a
2	ATF3	chr11:33793892-33794112	K562	blood:	n/a	n/a
3	BACH1	chr11:33795607-33795742	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr11:33796427-33796678	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr11:33791273-33791286	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr11:33783059-33783443	GM12878	blood:	n/a	chr11:33783205-33783216
7	BATF	chr11:33797327-33797677	GM12878	blood:	n/a	chr11:33797541-33797552
8	BATF	chr11:33783075-33783382	GM12878	blood:	n/a	chr11:33783205-33783216
9	BHLHE40	chr11:33795500-33795727	K562	blood:	n/a	chr11:33795595-33795611
10	BHLHE40	chr11:33795609-33795771	HepG2	liver:	n/a	n/a
11	BHLHE40	chr11:33794427-33794577	K562	blood:	n/a	n/a
12	BHLHE40	chr11:33795160-33795328	GM12878	blood:	n/a	n/a
13	BRCA1	chr11:33795928-33796002	HepG2	liver:	n/a	n/a
14	BRCA1	chr11:33796192-33796371	Hela-S3	cervix:	n/a	n/a
15	CCNT2	chr11:33795454-33796326	K562	blood:	n/a	chr11:33795863-33795872 chr11:33795908-33795917
16	CEBPB	chr11:33796036-33796335	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr11:33795975-33796462	A549	lung:	n/a	chr11:33796330-33796341
18	CEBPB	chr11:33795965-33796502	Hela-S3	cervix:	n/a	chr11:33796330-33796341
19	CEBPB	chr11:33796110-33796251	HepG2	liver:	n/a	n/a
20	CEBPB	chr11:33796071-33796362	HepG2	liver:	n/a	chr11:33796330-33796341
21	CEBPB	chr11:33796057-33796447	K562	blood:	n/a	chr11:33796330-33796341
22	CEBPB	chr11:33795241-33795423	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr11:33793011-33793018	K562	blood:	n/a	n/a
24	CEBPB	chr11:33796004-33796493	A549	lung:	n/a	chr11:33796330-33796341
25	CEBPB	chr11:33796064-33796210	K562	blood:	n/a	n/a
26	CEBPB	chr11:33795929-33796434	MCF-7	breast:	n/a	chr11:33796330-33796341
27	CEBPB	chr11:33796060-33796328	K562	blood:	n/a	n/a
28	CEBPD	chr11:33795824-33796038	HepG2	liver:	n/a	n/a
29	CHD1	chr11:33796370-33796562	GM12878	blood:	n/a	n/a
30	CHD2	chr11:33795666-33796466	Hela-S3	cervix:	n/a	n/a
31	CHD2	chr11:33795482-33796696	GM12878	blood:	n/a	n/a
32	CHD2	chr11:33796248-33796379	HepG2	liver:	n/a	n/a
33	CHD2	chr11:33797101-33797166	GM12878	blood:	n/a	n/a
34	CHD2	chr11:33795223-33795615	K562	blood:	n/a	n/a
35	CHD2	chr11:33795887-33796448	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr11:33796025-33796436	K562	blood:	n/a	n/a
37	CREB1	chr11:33796084-33796380	A549	lung:	n/a	n/a
38	CTCF	chr11:33795680-33795830	SK-N-SH_RA	brain:	n/a	n/a
39	CTCF	chr11:33795100-33795250	GM12864	blood:	n/a	n/a
40	CTCF	chr11:33795100-33795250	HCFaa	heart:	n/a	n/a
41	CTCF	chr11:33795080-33795230	HRE	kidney:	n/a	n/a
42	CTCF	chr11:33795060-33795210	AG09319	gingival:	n/a	n/a
43	CTCF	chr11:33795000-33795150	GM12869	blood:	n/a	n/a
44	CTCF	chr11:33794980-33795130	A549	lung:	n/a	n/a
45	CTCF	chr11:33795098-33795117	GM20000	blood:	n/a	n/a
46	CTCF	chr11:33795040-33795190	HMF	breast:	n/a	n/a
47	CTCF	chr11:33794000-33794150	SAEC	small airway:	n/a	n/a
48	CTCF	chr11:33795078-33795141	GM13976	blood:	n/a	n/a
49	CTCF	chr11:33794965-33795344	GM12878	blood:	n/a	n/a
50	CTCF	chr11:33795000-33795150	GM06990	blood:	n/a	n/a

(count:859 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:33796038-33796088	SAEC	small airway:	n/a
2	chr11:33796187-33796237	HEEpiC	esophagus:	n/a
3	chr11:33792972-33793022	HRPEpiC	eye:	n/a
4	chr11:33796225-33796275	SKMC	muscle:	n/a
5	chr11:33796257-33796307	Caco-2	colon:	n/a
6	chr11:33796038-33796088	SAEC	small airway:	n/a
7	chr11:33796187-33796237	HEEpiC	esophagus:	n/a
8	chr11:33792972-33793022	HRPEpiC	eye:	n/a
9	chr11:33796225-33796275	SKMC	muscle:	n/a
10	chr11:33796257-33796307	Caco-2	colon:	n/a
11	chr11:33796038-33796088	HPAEpiC	pulmonary alveolar:	n/a
12	chr11:33796228-33796278	GM19239	blood:	n/a
13	chr11:33797161-33797211	AG09319	gingival:	n/a
14	chr11:33796106-33796156	HEK293	kidney:	embryo
15	chr11:33795713-33795763	HPAEpiC	pulmonary alveolar:	n/a
16	chr11:33796228-33796278	U87	brain:	n/a
17	chr11:33796225-33796275	NT2-D1	testis:	n/a
18	chr11:33797161-33797211	AG10803	skin:	n/a
19	chr11:33796228-33796278	NH-A	brain:	n/a
20	chr11:33795595-33795645	NB4	blood:	n/a
21	chr11:33795924-33795974	HCT-116	colon:	n/a
22	chr11:33796225-33796275	HRE	kidney:	n/a
23	chr11:33796228-33796278	HCPEpiC	choroid plexus:	n/a
24	chr11:33796038-33796088	PANC-1	pancreas:	n/a
25	chr11:33796235-33796285	SKMC	muscle:	n/a
26	chr11:33796235-33796285	AG04449	skin:	fetal
27	chr11:33796038-33796088	H1-hESC	embryonic stem cell:	embryo
28	chr11:33796038-33796088	SK-N-SH	brain:	n/a
29	chr11:33792972-33793022	T-47D	breast:	n/a
30	chr11:33795713-33795763	T-47D	breast:	n/a
31	chr11:33796257-33796307	HCPEpiC	choroid plexus:	n/a
32	chr11:33795713-33795763	HAEpiC	amniotic membrane:	n/a
33	chr11:33795595-33795645	HCM	heart:	n/a
34	chr11:33796187-33796237	GM19239	blood:	n/a
35	chr11:33796228-33796278	PrEC	prostate:	n/a
36	chr11:33796257-33796307	HMEC	breast:	n/a
37	chr11:33796038-33796088	ovcar-3	ovarian:	n/a
38	chr11:33796187-33796237	Caco-2	colon:	n/a
39	chr11:33796106-33796156	Hepatocyte	liver:	n/a
40	chr11:33796038-33796088	HUVEC	blood vessel:	n/a
41	chr11:33797161-33797211	SK-N-SH_RA	brain:	n/a
42	chr11:33796038-33796088	MCF10A-Er-Src	breast:	n/a
43	chr11:33795236-33795286	HEK293	kidney:	embryo
44	chr11:33796038-33796088	HCF	heart:	n/a
45	chr11:33796289-33796339	K562	blood:	n/a
46	chr11:33797161-33797211	GM12891	blood:	n/a
47	chr11:33796106-33796156	Hela-S3	cervix:	n/a
48	chr11:33796235-33796285	U87	brain:	n/a
49	chr11:33796187-33796237	MCF10A-Er-Src	breast:	n/a
50	chr11:33795595-33795645	SK-N-MC	brain:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:33770157..33771745-chr11:33780759..33782708,2	K562	blood:
2	chr11:33772508..33775389-chr11:33783928..33785925,2	MCF-7	breast:
3	chr11:33758430..33760609-chr11:33786708..33788444,2	K562	blood:
4	chr11:33780255..33782060-chr11:33788387..33790193,2	K562	blood:
5	chr11:33777788..33782173-chr11:33783108..33786558,6	K562	blood:
6	chr11:33756710..33758910-chr11:33782406..33785042,2	K562	blood:
7	chr1:201979413..201979986-chr11:33795913..33796432,2	HCT-116	colon:
8	chr11:33720701..33723094-chr11:33794886..33797220,2	MCF-7	breast:
9	chr11:33777788..33782173-chr11:33783108..33786558,6	K562	blood:
10	chr11:33787714..33789411-chr11:33793527..33796515,2	MCF-7	breast:
11	chr11:33785223..33786784-chr11:33794755..33796851,2	MCF-7	breast:
12	chr11:33784551..33787595-chr11:33793972..33796128,3	K562	blood:
13	chr11:33786160..33788052-chr11:33788330..33790900,2	K562	blood:
14	chr11:33795562..33796149-chr20:35402028..35402855,2	Hela-S3	cervix:
15	chr11:33756399..33761777-chr11:33794455..33799644,9	K562	blood:
16	chr11:33772540..33774284-chr11:33775913..33777575,2	K562	blood:
17	chr11:33782349..33784832-chr11:33794680..33796860,3	MCF-7	breast:
18	chr11:33786160..33788052-chr11:33788330..33790900,2	K562	blood:
19	chr11:33780255..33782060-chr11:33788387..33790193,2	K562	blood:
20	chr11:33741351..33743266-chr11:33784029..33786297,2	MCF-7	breast:
21	chr11:33757743..33759681-chr11:33794774..33797554,2	MCF-7	breast:
22	chr11:33772286..33774284-chr11:33776075..33777715,2	K562	blood:
23	chr11:33756496..33759717-chr11:33794342..33798618,4	K562	blood:
24	chr11:33783005..33784901-chr11:33798617..33800423,2	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C11orf41-2	chr11:33796800-33796909	ENSG00000254508.1
2	lnc-C11orf41-2	chr11:33796994-33797216	ENSG00000254508.1
3	lnc-C11orf41-2	chr11:33796154-33796297	NONHSAT018716
4	lnc-C11orf41-2	chr11:33796245-33796297	ENSG00000254508.1
5	lnc-C11orf41-2	chr11:33796800-33797428	NONHSAT018716
6	lnc-C11orf41-2	chr11:33796800-33796909	ENSG00000254508.1
7	lnc-C11orf41-2	chr11:33796998-33797216	ENSG00000254508.1
8	lnc-C11orf41-2	chr11:33796251-33796297	ENSG00000254508.1
9	lnc-C11orf41-2	chr11:33796189-33796297	NONHSAT018717
10	lnc-C11orf41-2	chr11:33796797-33797216	NONHSAT018717

No data

Variant related genes	Relation type
ENSG00000254508	TF binding region
ENSG00000255272	TF binding region
FBXO3	TF binding region
ENSG00000254508	CpG island
ENSG00000255272	CpG island
FBXO3	CpG island
ENSG00000110429	chromatin interactions
ENSG00000205177	chromatin interactions
ENSG00000234678	chromatin interactions
ENSG00000149636	chromatin interactions
ENSG00000085063	chromatin interactions
ENSG00000163435	chromatin interactions
ENSG00000254508	chromatin interactions

Extended variants
information (count: 686 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:686 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1402954	chr11:33777334-33777335	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs557743553	chr11:33777368-33777369	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs151045343	chr11:33777371-33777372	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs149827586	chr11:33777373-33777374	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs371527457	chr11:33777386-33777387	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs112952452	chr11:33777428-33777429	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs140984470	chr11:33777467-33777468	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs145079432	chr11:33777503-33777504	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs571222003	chr11:33777529-33777530	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs201975557	chr11:33777540-33777541	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs527241421	chr11:33777555-33777556	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs547739627	chr11:33777560-33777561	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs377051654	chr11:33777565-33777566	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs111528975	chr11:33777578-33777579	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs536537212	chr11:33777618-33777619	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs200028311	chr11:33777665-33777666	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs191243767	chr11:33777668-33777669	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs375020485	chr11:33777711-33777712	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs556365868	chr11:33777730-33777731	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs112218779	chr11:33777753-33777754	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs113655385	chr11:33777802-33777803	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs546946540	chr11:33777856-33777857	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs145841239	chr11:33777883-33777884	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs558741769	chr11:33777937-33777938	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs572124105	chr11:33777982-33777983	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs76928082	chr11:33777991-33777992	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs549437892	chr11:33778041-33778042	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs554521230	chr11:33778077-33778078	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs199556780	chr11:33778210-33778211	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs564909810	chr11:33778256-33778257	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs534229040	chr11:33778296-33778297	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs574827370	chr11:33778381-33778382	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs543696915	chr11:33778407-33778408	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs114571362	chr11:33778411-33778412	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs577317177	chr11:33778424-33778425	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs545094498	chr11:33778486-33778487	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs564790998	chr11:33778509-33778510	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs527363055	chr11:33778527-33778528	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs547453527	chr11:33778552-33778553	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs368047844	chr11:33778561-33778562	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs372130031	chr11:33778569-33778570	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs372338120	chr11:33778581-33778582	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs549763859	chr11:33778615-33778616	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs569842694	chr11:33778634-33778635	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs183100071	chr11:33778638-33778639	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs12224154	chr11:33778729-33778730	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs565864815	chr11:33778749-33778750	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs369183750	chr11:33778765-33778766	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs565852515	chr11:33778782-33778783	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs34944910	chr11:33778831-33778832	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:77)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Medulloblastoma	16783165	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18194544	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	21364760	CNVD
Aniridia syndrome	21572526	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Retinoblastoma	22278416	CNVD
Denys-drash syndrome	21085971	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
WAGR syndrome	16773131	CNVD
Disorders of sex development	22290220	CNVD
Aniridia syndrome	17204608	CNVD
Mental retardation	17204608	CNVD
WAGR syndrome	19617690	CNVD
genitourinary abnormalities	17204608	CNVD
Breast cancer	16397240	CNVD
Mental retardation	16773131	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Cancer	21183584	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
WAGR syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Denys-drash syndrome	19566914	CNVD
Familial wilms tumor	19566914	CNVD
Frasier syndrome	19566914	CNVD
Non-small cell lung cancer	21829676	CNVD
WAGR syndrome	20603712	CNVD
Autism	17322880	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21858162	CNVD
Cancer	20164920	CNVD
Breast cancer	16620391	CNVD

Chromatin state (count:1244 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:33758800-33795000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr11:33759000-33778400	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr11:33759000-33780800	Weak transcription	Psoas Muscle	Psoas
4	chr11:33759000-33781000	Weak transcription	Fetal Brain Male	brain
5	chr11:33759000-33795200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr11:33759400-33778200	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr11:33760400-33785200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr11:33763200-33792200	Strong transcription	Fetal Thymus	thymus
9	chr11:33763200-33792400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr11:33764000-33781600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr11:33764200-33792000	Strong transcription	Primary T helper cells fromperipheralblood	blood
12	chr11:33764400-33791200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
13	chr11:33764400-33792200	Strong transcription	Primary monocytes fromperipheralblood	blood
14	chr11:33764400-33792400	Strong transcription	Primary T cells fromperipheralblood	blood
15	chr11:33764400-33792400	Strong transcription	Monocytes-CD14+_RO01746	blood
16	chr11:33764600-33785200	Strong transcription	Primary T helper cells PMA-I stimulated	--
17	chr11:33765200-33778400	Weak transcription	Pancreas	Pancrea
18	chr11:33765200-33780000	Weak transcription	Right Ventricle	heart
19	chr11:33765200-33785800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr11:33765400-33780000	Weak transcription	Aorta	Aorta
21	chr11:33765400-33793800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr11:33766600-33787600	Weak transcription	Stomach Mucosa	stomach
23	chr11:33767000-33779000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr11:33767200-33780800	Weak transcription	HepG2	liver
25	chr11:33767400-33791400	Strong transcription	Placenta	Placenta
26	chr11:33767600-33785800	Weak transcription	HUES6 Cell Line	embryonic stem cell
27	chr11:33767600-33792400	Strong transcription	Primary neutrophils fromperipheralblood	blood
28	chr11:33767800-33781000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr11:33767800-33784000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr11:33767800-33784600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
31	chr11:33767800-33785800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr11:33767800-33792200	Strong transcription	Adipose Nuclei	Adipose
33	chr11:33767800-33792400	Strong transcription	Primary B cells from peripheral blood	blood
34	chr11:33768000-33785800	Weak transcription	Small Intestine	intestine
35	chr11:33768200-33780000	Weak transcription	K562	blood
36	chr11:33769000-33782200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
37	chr11:33769600-33783800	Strong transcription	Rectal Mucosa Donor 29	rectum
38	chr11:33769600-33795000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr11:33769800-33780800	Weak transcription	Pancreatic Islets	Pancreatic Islet
40	chr11:33770000-33780000	Weak transcription	A549	lung
41	chr11:33770200-33791200	Strong transcription	Liver	Liver
42	chr11:33770400-33789200	Weak transcription	NHLF	lung
43	chr11:33770800-33791600	Strong transcription	Duodenum Mucosa	Duodenum
44	chr11:33771000-33779000	Strong transcription	Brain Hippocampus Middle	brain
45	chr11:33771200-33778000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr11:33772200-33785800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
47	chr11:33772600-33785400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr11:33774400-33779000	Strong transcription	Primary T cells from cord blood	blood
49	chr11:33774400-33779800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr11:33774400-33782400	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood

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