Variant report

Variant	nsv898178
Chromosome Location	chr11:92881933-92949447
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:940)
CpG islands
(count:733)
Chromatin interactive
region (count:20)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:940 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:92930141-92931015	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:92903235-92903466	K562	blood:	n/a	n/a
3	ARID3A	chr11:92903283-92903384	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	chr11:92930348-92930835	K562	blood:	n/a	chr11:92930622-92930636
8	BACH1	chr11:92930194-92931093	H1-hESC	embryonic stem cell:	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	chr11:92926939-92927228	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr11:92926906-92927262	A549	lung:	n/a	n/a
22	CEBPB	chr11:92902324-92902661	A549	lung:	n/a	chr11:92902468-92902479
23	CEBPB	chr11:92914385-92914488	K562	blood:	n/a	n/a
24	CEBPB	chr11:92931063-92931432	K562	blood:	n/a	n/a
25	CEBPB	chr11:92932822-92933072	A549	lung:	n/a	n/a
26	CEBPB	chr11:92931022-92931443	MCF-7	breast:	n/a	n/a
27	CEBPB	chr11:92930611-92931454	HepG2	liver:	n/a	n/a
28	CEBPB	chr11:92902286-92902674	Hela-S3	cervix:	n/a	chr11:92902468-92902479
29	CEBPB	chr11:92931021-92931462	HepG2	liver:	n/a	n/a
30	CEBPB	chr11:92930453-92931433	IMR90	lung:	n/a	n/a
31	CEBPB	chr11:92902294-92902662	K562	blood:	n/a	chr11:92902468-92902479
32	CEBPB	chr11:92930552-92930793	K562	blood:	n/a	n/a
33	CEBPB	chr11:92902254-92902666	A549	lung:	n/a	chr11:92902468-92902479
34	CEBPB	chr11:92926853-92927287	A549	lung:	n/a	n/a
35	CEBPB	chr11:92926904-92927280	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr11:92926904-92927274	IMR90	lung:	n/a	n/a
37	CEBPB	chr11:92931064-92931451	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr11:92926895-92927267	K562	blood:	n/a	n/a
39	CEBPB	chr11:92931039-92931453	A549	lung:	n/a	n/a
40	CEBPB	chr11:92931084-92931342	HepG2	liver:	n/a	n/a
41	CEBPB	chr11:92902294-92902665	IMR90	lung:	n/a	chr11:92902468-92902479
42	CEBPB	chr11:92902285-92902616	H1-hESC	embryonic stem cell:	n/a	chr11:92902468-92902479
43	CEBPB	chr11:92926914-92927273	HepG2	liver:	n/a	n/a
44	CEBPB	chr11:92929971-92931626	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr11:92931051-92931422	A549	lung:	n/a	n/a
46	CEBPB	chr11:92930607-92931450	HepG2	liver:	n/a	n/a
47	CEBPB	chr11:92931053-92931431	K562	blood:	n/a	n/a
48	CEBPB	chr11:92931003-92931553	A549	lung:	n/a	n/a
49	CEBPB	chr11:92902299-92902653	HepG2	liver:	n/a	chr11:92902468-92902479
50	CEBPD	chr11:92930947-92931319	HepG2	liver:	n/a	n/a

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:92928169-92928219	PANC-1	pancreas:	n/a
2	chr11:92928169-92928219	PANC-1	pancreas:	n/a
3	chr11:92931280-92931330	AoSMC	blood vessel:	n/a
4	chr11:92931416-92931466	HCF	heart:	n/a
5	chr11:92931304-92931354	K562	blood:	n/a
6	chr11:92930916-92930966	LNCaP	prostate:	n/a
7	chr11:92931311-92931361	U87	brain:	n/a
8	chr11:92931390-92931440	AoSMC	blood vessel:	n/a
9	chr11:92931304-92931354	H1-hESC	embryonic stem cell:	embryo
10	chr11:92931304-92931354	BJ	skin:	n/a
11	chr11:92931311-92931361	HEEpiC	esophagus:	n/a
12	chr11:92931250-92931300	MCF10A-Er-Src	breast:	n/a
13	chr11:92930990-92931040	HAEpiC	amniotic membrane:	n/a
14	chr11:92930777-92930827	GM19239	blood:	n/a
15	chr11:92928169-92928219	SAEC	small airway:	n/a
16	chr11:92930916-92930966	SAEC	small airway:	n/a
17	chr11:92931280-92931330	HUVEC	blood vessel:	n/a
18	chr11:92931304-92931354	PANC-1	pancreas:	n/a
19	chr11:92930739-92930789	A549	lung:	n/a
20	chr11:92931304-92931354	MCF-7	breast:	n/a
21	chr11:92931250-92931300	CMK	blood:	n/a
22	chr11:92930990-92931040	ovcar-3	ovarian:	n/a
23	chr11:92930777-92930827	NB4	blood:	n/a
24	chr11:92930739-92930789	PANC-1	pancreas:	n/a
25	chr11:92925402-92925452	CMK	blood:	n/a
26	chr11:92930990-92931040	HCPEpiC	choroid plexus:	n/a
27	chr11:92931280-92931330	Hela-S3	cervix:	n/a
28	chr11:92930739-92930789	SAEC	small airway:	n/a
29	chr11:92928169-92928219	RPTEC	kidney:	n/a
30	chr11:92931416-92931466	PrEC	prostate:	n/a
31	chr11:92925402-92925452	AG04450	lung:	fetal
32	chr11:92931280-92931330	NHDF-neo	bronchial:	n/a
33	chr11:92931250-92931300	HNPCEpiC	eye:	n/a
34	chr11:92930990-92931040	SK-N-SH_RA	brain:	n/a
35	chr11:92931311-92931361	HEK293	kidney:	embryo
36	chr11:92931250-92931300	PANC-1	pancreas:	n/a
37	chr11:92930990-92931040	SAEC	small airway:	n/a
38	chr11:92930916-92930966	HEEpiC	esophagus:	n/a
39	chr11:92925402-92925452	HPAEpiC	pulmonary alveolar:	n/a
40	chr11:92930777-92930827	SK-N-SH_RA	brain:	n/a
41	chr11:92930777-92930827	AG10803	skin:	n/a
42	chr11:92931416-92931466	HMEC	breast:	n/a
43	chr11:92930916-92930966	U87	brain:	n/a
44	chr11:92931304-92931354	RPTEC	kidney:	n/a
45	chr11:92930739-92930789	HEEpiC	esophagus:	n/a
46	chr11:92931416-92931466	AG04450	lung:	fetal
47	chr11:92931250-92931300	HL-60	blood:	n/a
48	chr11:92931311-92931361	BJ	skin:	n/a
49	chr11:92931250-92931300	NT2-D1	testis:	n/a
50	chr11:92928169-92928219	HNPCEpiC	eye:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr11:92922677..92925407-chr11:92931500..92933970,2	K562	blood:
2	chr11:92930280..92930897-chr13:21750350..21750876,2	NB4	blood:
3	chr11:92926307..92929305-chr11:92932606..92934275,2	K562	blood:
4	chr11:92923610..92925179-chr11:92926735..92930108,3	K562	blood:
5	chr11:92929754..92932156-chr11:92932855..92934960,2	K562	blood:
6	chr11:92929302..92933098-chr11:92935947..92940033,5	K562	blood:
7	chr11:92895585..92897529-chr11:92904062..92906165,2	K562	blood:
8	chr1:9599460..9600393-chr11:92930413..92931236,2	NB4	blood:
9	chr11:92923126..92925110-chr11:92926233..92928235,2	K562	blood:
10	chr11:92923126..92925110-chr11:92926233..92928235,2	K562	blood:
11	chr11:92923610..92925179-chr11:92926735..92930108,3	K562	blood:
12	chr11:92926307..92929305-chr11:92932606..92934275,2	K562	blood:
13	chr11:92930510..92931167-chr7:75677293..75677907,2	NB4	blood:
14	chr11:92921750..92923614-chr11:92929621..92931321,2	K562	blood:
15	chr11:92922677..92925407-chr11:92931500..92933970,2	K562	blood:
16	chr11:92922649..92925580-chr11:92928547..92930821,3	MCF-7	breast:
17	chr11:92930328..92931259-chr17:73775093..73776047,2	Hela-S3	cervix:
18	chr11:92895585..92897529-chr11:92904062..92906165,2	K562	blood:
19	chr11:92927495..92929047-chr11:92961405..92963884,2	K562	blood:
20	chr11:92926707..92928673-chr11:92929103..92931682,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MTNR1B-3	chr11:92885241-92885916	NONHSAT023640

No data

Variant related genes	Relation type
SLC36A4	TF binding region
ENSG00000255445	TF binding region
SLC36A4	CpG island
ENSG00000255445	CpG island
ENSG00000165480	chromatin interactions
ENSG00000180773	chromatin interactions
ENSG00000171612	chromatin interactions
ENSG00000127952	chromatin interactions
ENSG00000146701	chromatin interactions
ENSG00000173141	chromatin interactions
ENSG00000132475	chromatin interactions

Extended variants
information (count: 1930 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:1930 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17854443	chr11:92881933-92881934	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs571218674	chr11:92881961-92881962	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs138573173	chr11:92881963-92881964	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs267603248	chr11:92881964-92881965	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs200976617	chr11:92881986-92881987	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs77563026	chr11:92882005-92882006	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs149302069	chr11:92882006-92882007	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs368119386	chr11:92882029-92882030	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs536467473	chr11:92882088-92882089	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs3758676	chr11:92882096-92882097	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs371846273	chr11:92882132-92882133	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs572809882	chr11:92882136-92882137	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs554789166	chr11:92882148-92882149	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs369908225	chr11:92882155-92882156	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs112229297	chr11:92882209-92882210	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs573279295	chr11:92882214-92882215	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs558574535	chr11:92882247-92882248	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs560635690	chr11:92882322-92882323	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs140726865	chr11:92882352-92882353	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs540381065	chr11:92882378-92882379	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs144588205	chr11:92882467-92882468	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs116604332	chr11:92882508-92882509	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs542458901	chr11:92882548-92882549	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs555752762	chr11:92882620-92882621	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs10466352	chr11:92882623-92882624	Weak transcription Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs11020180	chr11:92882648-92882649	Weak transcription Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs115495021	chr11:92882787-92882788	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs117954333	chr11:92882794-92882795	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs532109323	chr11:92882820-92882821	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs550277793	chr11:92882871-92882872	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs181584226	chr11:92882908-92882909	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs147853309	chr11:92882917-92882918	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs527910448	chr11:92882931-92882932	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs148914152	chr11:92882978-92882979	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs566327297	chr11:92882981-92882982	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs533874437	chr11:92883024-92883025	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs558414321	chr11:92883034-92883035	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs533501294	chr11:92883055-92883056	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs577196669	chr11:92883081-92883082	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs75441298	chr11:92883104-92883105	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs200013867	chr11:92883105-92883106	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs200282207	chr11:92883106-92883107	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs544617591	chr11:92883178-92883179	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs185857911	chr11:92883212-92883213	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs375958747	chr11:92883241-92883242	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs78199822	chr11:92883253-92883254	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs142690868	chr11:92883292-92883293	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs560717307	chr11:92883293-92883294	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs538130091	chr11:92883311-92883312	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs527869571	chr11:92883332-92883333	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:1226 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:92867200-92896400	Weak transcription	Primary B cells from peripheral blood	blood
2	chr11:92868000-92889000	Weak transcription	Adipose Nuclei	Adipose
3	chr11:92868400-92914600	Weak transcription	Brain Substantia Nigra	brain
4	chr11:92875000-92892800	Weak transcription	Primary B cells from cord blood	blood
5	chr11:92875400-92910400	Weak transcription	Brain Cingulate Gyrus	brain
6	chr11:92876400-92896600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr11:92876600-92883800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr11:92876600-92885000	Weak transcription	Fetal Lung	lung
9	chr11:92876600-92885200	Weak transcription	Primary T cells from cord blood	blood
10	chr11:92876600-92900400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
11	chr11:92876600-92910600	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr11:92876800-92910600	Weak transcription	Lung	lung
13	chr11:92877000-92890400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr11:92877000-92911400	Weak transcription	Osteobl	bone
15	chr11:92877200-92890000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr11:92877200-92894800	Weak transcription	HSMM	muscle
17	chr11:92877800-92899600	Weak transcription	NHLF	lung
18	chr11:92877800-92915000	Weak transcription	Muscle Satellite Cultured Cells	--
19	chr11:92878000-92894600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr11:92878200-92888200	Strong transcription	Monocytes-CD14+_RO01746	blood
21	chr11:92878400-92887400	Strong transcription	Primary monocytes fromperipheralblood	blood
22	chr11:92878400-92910600	Weak transcription	Placenta Amnion	Placenta Amnion
23	chr11:92878600-92890800	Weak transcription	Left Ventricle	heart
24	chr11:92878800-92889200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr11:92878800-92890600	Weak transcription	Dnd41	blood
26	chr11:92878800-92893200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
27	chr11:92878800-92895800	Weak transcription	Brain Germinal Matrix	brain
28	chr11:92878800-92896000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
29	chr11:92879000-92889200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr11:92879000-92896600	Weak transcription	Ovary	ovary
31	chr11:92879000-92900200	Weak transcription	Fetal Muscle Leg	muscle
32	chr11:92879000-92910800	Weak transcription	HSMMtube	muscle
33	chr11:92879200-92890200	Weak transcription	Cortex derived primary cultured neurospheres	brain
34	chr11:92879200-92890400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr11:92879200-92892600	Weak transcription	Primary T cells fromperipheralblood	blood
36	chr11:92879200-92896600	Weak transcription	Fetal Brain Female	brain
37	chr11:92879400-92885200	Weak transcription	Liver	Liver
38	chr11:92879600-92882000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr11:92879600-92889200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
40	chr11:92879600-92890000	Weak transcription	Duodenum Smooth Muscle	Duodenum
41	chr11:92879600-92910000	Weak transcription	Fetal Brain Male	brain
42	chr11:92879600-92910800	Weak transcription	HMEC	breast
43	chr11:92880000-92882000	Strong transcription	Primary neutrophils fromperipheralblood	blood
44	chr11:92880000-92882600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr11:92880200-92894600	Weak transcription	Placenta	Placenta
46	chr11:92880400-92885800	Weak transcription	HUES48 Cell Line	embryonic stem cell
47	chr11:92880400-92886600	Weak transcription	HUES64 Cell Line	embryonic stem cell
48	chr11:92880400-92895800	Weak transcription	Brain Angular Gyrus	brain
49	chr11:92880800-92883200	Strong transcription	Hela-S3	cervix
50	chr11:92881000-92888400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links