Variant report

Variant	nsv818858
Chromosome Location	chr11:92898342-92932229
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:882)
CpG islands
(count:734)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:882 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:92903283-92903384	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:92903235-92903466	K562	blood:	n/a	n/a
3	ARID3A	chr11:92930141-92931015	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:92925428-92925626	K562	blood:	n/a	n/a
5	ATF1	chr11:92930464-92930811	K562	blood:	n/a	n/a
6	ATF3	chr11:92930439-92930795	K562	blood:	n/a	n/a
7	BACH1	chr11:92930194-92931093	H1-hESC	embryonic stem cell:	n/a	chr11:92930622-92930636
8	BACH1	chr11:92930348-92930835	K562	blood:	n/a	chr11:92930622-92930636
9	BACH1	chr11:92931235-92931313	K562	blood:	n/a	n/a
10	BATF	chr11:92930451-92930816	GM12878	blood:	n/a	n/a
11	BCLAF1	chr11:92930357-92931221	GM12878	blood:	n/a	chr11:92931040-92931053 chr11:92931044-92931057
12	BCLAF1	chr11:92930350-92931001	GM12878	blood:	n/a	n/a
13	BHLHE40	chr11:92930345-92930997	GM12878	blood:	n/a	n/a
14	BHLHE40	chr11:92930424-92931132	K562	blood:	n/a	chr11:92931043-92931059
15	BHLHE40	chr11:92930474-92931435	HepG2	liver:	n/a	chr11:92931043-92931059
16	BRCA1	chr11:92930149-92931654	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr11:92930869-92931186	HepG2	liver:	n/a	n/a
18	CBX3	chr11:92930416-92931063	K562	blood:	n/a	n/a
19	CCNT2	chr11:92930714-92931265	K562	blood:	n/a	n/a
20	CEBPB	chr11:92931021-92931462	HepG2	liver:	n/a	n/a
21	CEBPB	chr11:92902299-92902653	HepG2	liver:	n/a	chr11:92902468-92902479
22	CEBPB	chr11:92931051-92931422	A549	lung:	n/a	n/a
23	CEBPB	chr11:92902294-92902665	IMR90	lung:	n/a	chr11:92902468-92902479
24	CEBPB	chr11:92929971-92931626	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr11:92926914-92927273	HepG2	liver:	n/a	n/a
26	CEBPB	chr11:92931063-92931432	K562	blood:	n/a	n/a
27	CEBPB	chr11:92930453-92931433	IMR90	lung:	n/a	n/a
28	CEBPB	chr11:92902286-92902674	Hela-S3	cervix:	n/a	chr11:92902468-92902479
29	CEBPB	chr11:92902324-92902661	A549	lung:	n/a	chr11:92902468-92902479
30	CEBPB	chr11:92902254-92902666	A549	lung:	n/a	chr11:92902468-92902479
31	CEBPB	chr11:92926904-92927280	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr11:92926904-92927274	IMR90	lung:	n/a	n/a
33	CEBPB	chr11:92931003-92931553	A549	lung:	n/a	n/a
34	CEBPB	chr11:92930607-92931450	HepG2	liver:	n/a	n/a
35	CEBPB	chr11:92931039-92931453	A549	lung:	n/a	n/a
36	CEBPB	chr11:92902285-92902616	H1-hESC	embryonic stem cell:	n/a	chr11:92902468-92902479
37	CEBPB	chr11:92931053-92931431	K562	blood:	n/a	n/a
38	CEBPB	chr11:92926939-92927228	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr11:92926906-92927262	A549	lung:	n/a	n/a
40	CEBPB	chr11:92930611-92931454	HepG2	liver:	n/a	n/a
41	CEBPB	chr11:92902294-92902662	K562	blood:	n/a	chr11:92902468-92902479
42	CEBPB	chr11:92926853-92927287	A549	lung:	n/a	n/a
43	CEBPB	chr11:92931064-92931451	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr11:92931084-92931342	HepG2	liver:	n/a	n/a
45	CEBPB	chr11:92914385-92914488	K562	blood:	n/a	n/a
46	CEBPB	chr11:92926895-92927267	K562	blood:	n/a	n/a
47	CEBPB	chr11:92931022-92931443	MCF-7	breast:	n/a	n/a
48	CEBPB	chr11:92930552-92930793	K562	blood:	n/a	n/a
49	CEBPD	chr11:92930947-92931319	HepG2	liver:	n/a	n/a
50	CEBPD	chr11:92931047-92931403	HepG2	liver:	n/a	n/a

(count:734 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:92930916-92930966	HEK293	kidney:	embryo
2	chr11:92931390-92931440	K562	blood:	n/a
3	chr11:92930916-92930966	HEK293	kidney:	embryo
4	chr11:92931390-92931440	K562	blood:	n/a
5	chr11:92931416-92931466	A549	lung:	n/a
6	chr11:92931250-92931300	ECC-1	luminal epithelium:	n/a
7	chr11:92930777-92930827	HRE	kidney:	n/a
8	chr11:92930916-92930966	HRCEpiC	kidney:	n/a
9	chr11:92930777-92930827	Caco-2	colon:	n/a
10	chr11:92930990-92931040	U87	brain:	n/a
11	chr11:92931304-92931354	HCF	heart:	n/a
12	chr11:92931304-92931354	HRCEpiC	kidney:	n/a
13	chr11:92931304-92931354	NB4	blood:	n/a
14	chr11:92930916-92930966	RPTEC	kidney:	n/a
15	chr11:92931250-92931300	Hela-S3	cervix:	n/a
16	chr11:92925402-92925452	SAEC	small airway:	n/a
17	chr11:92931390-92931440	AG10803	skin:	n/a
18	chr11:92931304-92931354	Caco-2	colon:	n/a
19	chr11:92930990-92931040	MCF10A-Er-Src	breast:	n/a
20	chr11:92931390-92931440	PFSK-1	brain:	n/a
21	chr11:92930739-92930789	HCT-116	colon:	n/a
22	chr11:92931250-92931300	HMEC	breast:	n/a
23	chr11:92930990-92931040	HRPEpiC	eye:	n/a
24	chr11:92928169-92928219	HRPEpiC	eye:	n/a
25	chr11:92930990-92931040	RPTEC	kidney:	n/a
26	chr11:92931390-92931440	HCM	heart:	n/a
27	chr11:92931250-92931300	K562	blood:	n/a
28	chr11:92925402-92925452	HRCEpiC	kidney:	n/a
29	chr11:92928169-92928219	HCF	heart:	n/a
30	chr11:92930990-92931040	MCF-7	breast:	n/a
31	chr11:92931416-92931466	HCT-116	colon:	n/a
32	chr11:92928169-92928219	ovcar-3	ovarian:	n/a
33	chr11:92930990-92931040	HPAEpiC	pulmonary alveolar:	n/a
34	chr11:92930916-92930966	AG04450	lung:	fetal
35	chr11:92931416-92931466	NHBE	bronchial:	n/a
36	chr11:92930916-92930966	GM06990	blood:	n/a
37	chr11:92925402-92925452	Jurkat	blood:	n/a
38	chr11:92930916-92930966	Hepatocyte	liver:	n/a
39	chr11:92931311-92931361	GM12878	blood:	n/a
40	chr11:92931280-92931330	Hela-S3	cervix:	n/a
41	chr11:92931311-92931361	NB4	blood:	n/a
42	chr11:92931311-92931361	GM19239	blood:	n/a
43	chr11:92930777-92930827	HCM	heart:	n/a
44	chr11:92925402-92925452	HMEC	breast:	n/a
45	chr11:92931390-92931440	AoSMC	blood vessel:	n/a
46	chr11:92930916-92930966	AG04449	skin:	fetal
47	chr11:92930739-92930789	HepG2	liver:	n/a
48	chr11:92930916-92930966	HUVEC	blood vessel:	n/a
49	chr11:92930739-92930789	AG04449	skin:	fetal
50	chr11:92931416-92931466	GM12891	blood:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:92930328..92931259-chr17:73775093..73776047,2	Hela-S3	cervix:
2	chr11:92923610..92925179-chr11:92926735..92930108,3	K562	blood:
3	chr11:92930510..92931167-chr7:75677293..75677907,2	NB4	blood:
4	chr11:92930280..92930897-chr13:21750350..21750876,2	NB4	blood:
5	chr11:92926307..92929305-chr11:92932606..92934275,2	K562	blood:
6	chr1:9599460..9600393-chr11:92930413..92931236,2	NB4	blood:
7	chr11:92922649..92925580-chr11:92928547..92930821,3	MCF-7	breast:
8	chr11:92895585..92897529-chr11:92904062..92906165,2	K562	blood:
9	chr11:92927495..92929047-chr11:92961405..92963884,2	K562	blood:
10	chr11:92923126..92925110-chr11:92926233..92928235,2	K562	blood:
11	chr11:92921750..92923614-chr11:92929621..92931321,2	K562	blood:
12	chr11:92923610..92925179-chr11:92926735..92930108,3	K562	blood:
13	chr11:92923126..92925110-chr11:92926233..92928235,2	K562	blood:
14	chr11:92922677..92925407-chr11:92931500..92933970,2	K562	blood:
15	chr11:92926707..92928673-chr11:92929103..92931682,2	K562	blood:
16	chr11:92922677..92925407-chr11:92931500..92933970,2	K562	blood:

No data

Variant related genes	Relation type
SLC36A4	TF binding region
SLC36A4	CpG island
ENSG00000132475	chromatin interactions
ENSG00000165480	chromatin interactions
ENSG00000173141	chromatin interactions
ENSG00000171612	chromatin interactions
ENSG00000127952	chromatin interactions
ENSG00000180773	chromatin interactions
ENSG00000146701	chromatin interactions

Extended variants
information (count: 1088 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:1088 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4753436	chr11:92898342-92898343	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs540833379	chr11:92898392-92898393	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs565328813	chr11:92898393-92898394	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs577265831	chr11:92898539-92898540	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs117867110	chr11:92898550-92898551	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs551275324	chr11:92898573-92898574	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs537514265	chr11:92898668-92898669	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs74937450	chr11:92898711-92898712	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs563308855	chr11:92898719-92898720	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs184456058	chr11:92898741-92898742	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs548672518	chr11:92898801-92898802	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs567356792	chr11:92898895-92898896	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs34053812	chr11:92898899-92898900	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs544697199	chr11:92898946-92898947	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs534379417	chr11:92898951-92898952	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs79608266	chr11:92898952-92898953	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs571348533	chr11:92898979-92898980	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs538572026	chr11:92899006-92899007	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs371994148	chr11:92899062-92899063	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs575169784	chr11:92899068-92899069	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs149144596	chr11:92899086-92899087	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs536252456	chr11:92899089-92899090	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs200479590	chr11:92899092-92899093	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs201629054	chr11:92899144-92899145	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs146740031	chr11:92899159-92899160	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs376618592	chr11:92899179-92899180	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs371187395	chr11:92899192-92899193	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs573330278	chr11:92899240-92899241	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs540368517	chr11:92899380-92899381	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs139281476	chr11:92899400-92899401	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs577499745	chr11:92899413-92899414	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs570113594	chr11:92899426-92899427	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs144062304	chr11:92899499-92899500	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs541678207	chr11:92899506-92899507	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs530370342	chr11:92899553-92899554	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs7941228	chr11:92899589-92899590	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs560709556	chr11:92899612-92899613	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs528234477	chr11:92899615-92899616	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs546354514	chr11:92899763-92899764	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs560101959	chr11:92899830-92899831	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs575260168	chr11:92899936-92899937	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs149038185	chr11:92899970-92899971	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs544120937	chr11:92899992-92899993	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs189282327	chr11:92899994-92899995	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs550317101	chr11:92900080-92900081	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs193237921	chr11:92900139-92900140	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs376794010	chr11:92900145-92900146	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs184753720	chr11:92900173-92900174	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs80065749	chr11:92900227-92900228	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs79589356	chr11:92900236-92900237	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	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
Prostate cancer	18632612	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
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	22429812	CNVD
Breast cancer	16608533	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Renal cell carcinoma	18194544	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Mental retardation	21062444	CNVD
Cancer	21499728	CNVD
Breast cancer	19181860	CNVD
Breast cancer	17603634	CNVD
Mantle cell lymphoma	19029149	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Basal cell lymphoma	16790693	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1015 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:92868400-92914600	Weak transcription	Brain Substantia Nigra	brain
2	chr11:92875400-92910400	Weak transcription	Brain Cingulate Gyrus	brain
3	chr11:92876600-92900400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
4	chr11:92876600-92910600	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr11:92876800-92910600	Weak transcription	Lung	lung
6	chr11:92877000-92911400	Weak transcription	Osteobl	bone
7	chr11:92877800-92899600	Weak transcription	NHLF	lung
8	chr11:92877800-92915000	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr11:92878400-92910600	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr11:92879000-92900200	Weak transcription	Fetal Muscle Leg	muscle
11	chr11:92879000-92910800	Weak transcription	HSMMtube	muscle
12	chr11:92879600-92910000	Weak transcription	Fetal Brain Male	brain
13	chr11:92879600-92910800	Weak transcription	HMEC	breast
14	chr11:92881200-92899200	Weak transcription	NH-A	brain
15	chr11:92882000-92910600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr11:92885800-92910000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr11:92888000-92900000	Weak transcription	Fetal Kidney	kidney
18	chr11:92888400-92900600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
19	chr11:92889000-92899800	Strong transcription	Monocytes-CD14+_RO01746	blood
20	chr11:92889000-92900200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
21	chr11:92889600-92902200	Weak transcription	Fetal Intestine Large	intestine
22	chr11:92889800-92900200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
23	chr11:92889800-92911200	Weak transcription	Brain Inferior Temporal Lobe	brain
24	chr11:92889800-92913600	Weak transcription	Spleen	Spleen
25	chr11:92890000-92899600	Strong transcription	Primary monocytes fromperipheralblood	blood
26	chr11:92890400-92901400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr11:92890400-92901800	Strong transcription	HUES64 Cell Line	embryonic stem cell
28	chr11:92890400-92910000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr11:92890600-92901400	Strong transcription	Dnd41	blood
30	chr11:92890600-92911600	Weak transcription	Colon Smooth Muscle	Colon
31	chr11:92890800-92900800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr11:92891200-92899000	Weak transcription	NHEK	skin
33	chr11:92891200-92903800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr11:92891400-92900400	Weak transcription	GM12878-XiMat	blood
35	chr11:92891600-92925400	Weak transcription	Fetal Heart	heart
36	chr11:92891800-92910800	Weak transcription	Right Ventricle	heart
37	chr11:92891800-92929800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
38	chr11:92892000-92910800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
39	chr11:92892400-92901400	Strong transcription	Primary neutrophils fromperipheralblood	blood
40	chr11:92892600-92900000	Strong transcription	Primary T cells fromperipheralblood	blood
41	chr11:92892600-92901000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr11:92892600-92902400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr11:92892600-92910400	Weak transcription	Fetal Muscle Trunk	muscle
44	chr11:92892800-92901400	Strong transcription	Primary B cells from cord blood	blood
45	chr11:92893000-92900800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr11:92893200-92901400	Strong transcription	HUES6 Cell Line	embryonic stem cell
47	chr11:92893200-92910600	Weak transcription	Rectal Mucosa Donor 29	rectum
48	chr11:92893600-92898400	Strong transcription	Duodenum Smooth Muscle	Duodenum
49	chr11:92893600-92910400	Weak transcription	Skeletal Muscle Female	skeletal muscle
50	chr11:92893800-92910000	Weak transcription	Cortex derived primary cultured neurospheres	brain

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