Variant report

Variant	esv1844274
Chromosome Location	chr11:86776992-86872908
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:708)
CpG islands
(count:61)
Chromatin interactive
region (count:29)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:708 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:86808565-86809024	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:86808596-86809092	K562	blood:	n/a	n/a
3	ARID3A	chr11:86861511-86861769	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:86787689-86788620	HepG2	liver:	n/a	n/a
5	ARID3A	chr11:86839305-86839814	HepG2	liver:	n/a	n/a
6	ATF1	chr11:86808580-86808925	K562	blood:	n/a	n/a
7	ATF3	chr11:86803222-86803489	K562	blood:	n/a	n/a
8	BACH1	chr11:86805450-86805451	K562	blood:	n/a	n/a
9	BACH1	chr11:86808725-86808892	K562	blood:	n/a	n/a
10	BACH1	chr11:86835199-86835457	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr11:86859343-86859398	H1-hESC	embryonic stem cell:	n/a	n/a
12	BCL11A	chr11:86794104-86794296	H1-hESC	embryonic stem cell:	n/a	n/a
13	BCL11A	chr11:86794117-86794402	H1-hESC	embryonic stem cell:	n/a	n/a
14	BHLHE40	chr11:86808720-86808888	K562	blood:	n/a	n/a
15	BRCA1	chr11:86794111-86794566	H1-hESC	embryonic stem cell:	n/a	n/a
16	CBX3	chr11:86797796-86798165	K562	blood:	n/a	n/a
17	CBX3	chr11:86808476-86808990	K562	blood:	n/a	n/a
18	CCNT2	chr11:86808679-86808904	K562	blood:	n/a	n/a
19	CEBPB	chr11:86803289-86803589	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr11:86788183-86788372	A549	lung:	n/a	n/a
21	CEBPB	chr11:86836336-86836649	A549	lung:	n/a	n/a
22	CEBPB	chr11:86861546-86861748	HepG2	liver:	n/a	n/a
23	CEBPB	chr11:86836241-86836797	A549	lung:	n/a	n/a
24	CEBPB	chr11:86848820-86848896	HepG2	liver:	n/a	n/a
25	CEBPB	chr11:86787970-86788282	HepG2	liver:	n/a	chr11:86788171-86788182
26	CEBPB	chr11:86814685-86814880	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr11:86832702-86832814	K562	blood:	n/a	n/a
28	CEBPB	chr11:86803287-86803608	K562	blood:	n/a	n/a
29	CEBPB	chr11:86811816-86811879	K562	blood:	n/a	n/a
30	CEBPB	chr11:86787984-86788286	HepG2	liver:	n/a	chr11:86788171-86788182
31	CEBPB	chr11:86832701-86832770	A549	lung:	n/a	n/a
32	CEBPB	chr11:86787785-86788447	HepG2	liver:	n/a	chr11:86788171-86788182
33	CEBPB	chr11:86836311-86836703	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr11:86787987-86788269	HepG2	liver:	n/a	chr11:86788171-86788182
35	CEBPB	chr11:86831217-86831245	HepG2	liver:	n/a	n/a
36	CEBPB	chr11:86855298-86855577	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr11:86823041-86823150	HepG2	liver:	n/a	n/a
38	CEBPB	chr11:86788105-86788362	K562	blood:	n/a	chr11:86788171-86788182
39	CEBPB	chr11:86826542-86826650	K562	blood:	n/a	chr11:86826604-86826617 chr11:86826604-86826617 chr11:86826606-86826615 chr11:86826606-86826615 chr11:86826604-86826617 chr11:86826606-86826615 chr11:86826606-86826615 chr11:86826604-86826615 chr11:86826604-86826615
40	CEBPB	chr11:86814348-86814868	K562	blood:	n/a	n/a
41	CEBPD	chr11:86787999-86788204	HepG2	liver:	n/a	n/a
42	CHD1	chr11:86794598-86794704	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD2	chr11:86808615-86808994	K562	blood:	n/a	n/a
44	CTCF	chr11:86808640-86808790	GM12865	blood:	n/a	n/a
45	CTCF	chr11:86807033-86807209	ProgFib	skin:	n/a	n/a
46	CTCF	chr11:86808680-86808830	BE2_C	brain:	n/a	n/a
47	CTCF	chr11:86808616-86808883	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr11:86808680-86808830	WERI-Rb-1	eye:	n/a	n/a
49	CTCF	chr11:86807120-86807270	NHLF	lung:	n/a	n/a
50	CTCF	chr11:86807040-86807190	AG09309	skin:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:86793667-86793717	K562	blood:	n/a
2	chr11:86793667-86793717	RPTEC	kidney:	n/a
3	chr11:86793667-86793717	Jurkat	blood:	n/a
4	chr11:86793667-86793717	NHDF-neo	bronchial:	n/a
5	chr11:86793667-86793717	SKMC	muscle:	n/a
6	chr11:86793667-86793717	AG04450	lung:	fetal
7	chr11:86793667-86793717	Hela-S3	cervix:	n/a
8	chr11:86793667-86793717	NB4	blood:	n/a
9	chr11:86793667-86793717	ECC-1	luminal epithelium:	n/a
10	chr11:86793667-86793717	HRPEpiC	eye:	n/a
11	chr11:86793667-86793717	ovcar-3	ovarian:	n/a
12	chr11:86793667-86793717	GM12878	blood:	n/a
13	chr11:86793667-86793717	HRE	kidney:	n/a
14	chr11:86793667-86793717	H1-hESC	embryonic stem cell:	embryo
15	chr11:86793667-86793717	BE2_C	brain:	n/a
16	chr11:86793667-86793717	HMEC	breast:	n/a
17	chr11:86793667-86793717	AG10803	skin:	n/a
18	chr11:86793667-86793717	CMK	blood:	n/a
19	chr11:86793667-86793717	MCF-7	breast:	n/a
20	chr11:86793667-86793717	GM06990	blood:	n/a
21	chr11:86793667-86793717	HCPEpiC	choroid plexus:	n/a
22	chr11:86793667-86793717	HCF	heart:	n/a
23	chr11:86793667-86793717	HCT-116	colon:	n/a
24	chr11:86793667-86793717	HAEpiC	amniotic membrane:	n/a
25	chr11:86793667-86793717	BJ	skin:	n/a
26	chr11:86793667-86793717	AG09309	skin:	n/a
27	chr11:86793667-86793717	NHBE	bronchial:	n/a
28	chr11:86793667-86793717	GM19239	blood:	n/a
29	chr11:86793667-86793717	HRCEpiC	kidney:	n/a
30	chr11:86793667-86793717	SAEC	small airway:	n/a
31	chr11:86793667-86793717	HEEpiC	esophagus:	n/a
32	chr11:86793667-86793717	HepG2	liver:	n/a
33	chr11:86793667-86793717	PANC-1	pancreas:	n/a
34	chr11:86793667-86793717	U87	brain:	n/a
35	chr11:86793667-86793717	PrEC	prostate:	n/a
36	chr11:86793667-86793717	PFSK-1	brain:	n/a
37	chr11:86793667-86793717	SK-N-MC	brain:	n/a
38	chr11:86793667-86793717	HCM	heart:	n/a
39	chr11:86793667-86793717	HEK293	kidney:	embryo
40	chr11:86793667-86793717	A549	lung:	n/a
41	chr11:86793667-86793717	LNCaP	prostate:	n/a
42	chr11:86793667-86793717	HNPCEpiC	eye:	n/a
43	chr11:86793667-86793717	HIPEpiC	eye:	n/a
44	chr11:86793667-86793717	ProgFib	skin:	n/a
45	chr11:86793667-86793717	GM12891	blood:	n/a
46	chr11:86793667-86793717	NT2-D1	testis:	n/a
47	chr11:86793667-86793717	SK-N-SH_RA	brain:	n/a
48	chr11:86793667-86793717	SK-N-SH	brain:	n/a
49	chr11:86793667-86793717	HPAEpiC	pulmonary alveolar:	n/a
50	chr11:86793667-86793717	NH-A	brain:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:86803340..86806124-chr11:86810035..86812567,2	K562	blood:
2	chr11:86664821..86667112-chr11:86824827..86827318,2	MCF-7	breast:
3	chr11:86810025..86812420-chr11:86813811..86815830,2	K562	blood:
4	chr11:86798772..86800664-chr11:86801632..86803429,2	K562	blood:
5	chr11:86805484..86807360-chr11:87007311..87009404,2	MCF-7	breast:
6	chr11:86779436..86781916-chr11:86820681..86823632,2	K562	blood:
7	chr11:86818728..86820494-chr11:86831907..86834474,2	K562	blood:
8	chr11:86809033..86811037-chr11:86814602..86817030,2	K562	blood:
9	chr11:86706337..86706967-chr11:86808249..86808967,2	K562	blood:
10	chr11:86806619..86807569-chr11:86992272..86993052,3	MCF-7	breast:
11	chr11:86798772..86800664-chr11:86801632..86803429,2	K562	blood:
12	chr11:86847845..86849686-chr11:86851887..86854201,2	MCF-7	breast:
13	chr11:86810025..86812420-chr11:86813811..86815830,2	K562	blood:
14	chr11:86867900..86869412-chr11:86871775..86874240,2	K562	blood:
15	chr11:86773350..86775874-chr11:86786933..86789262,2	K562	blood:
16	chr11:86779436..86781916-chr11:86820681..86823632,2	K562	blood:
17	chr11:86809033..86811037-chr11:86814602..86817030,2	K562	blood:
18	chr11:86803340..86806124-chr11:86810035..86812567,2	K562	blood:
19	chr11:86775970..86778427-chr11:86780728..86783153,2	MCF-7	breast:
20	chr11:86791713..86794335-chr11:86807155..86810110,2	K562	blood:
21	chr11:86666377..86668127-chr11:86777845..86780660,2	K562	blood:
22	chr11:86847845..86849686-chr11:86851887..86854201,2	MCF-7	breast:
23	chr11:86867900..86869412-chr11:86871775..86874240,2	K562	blood:
24	chr11:86774381..86776873-chr11:86783192..86784791,2	MCF-7	breast:
25	chr11:86840088..86842543-chr11:86845796..86847320,2	K562	blood:
26	chr11:86664322..86666678-chr11:86802389..86805418,3	MCF-7	breast:
27	chr11:86666646..86669098-chr11:86793601..86796453,2	MCF-7	breast:
28	chr11:86818728..86820494-chr11:86831907..86834474,2	K562	blood:
29	chr11:86840088..86842543-chr11:86845796..86847320,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FZD4-6	chr11:86805776-86807627	NONHSAT023514

No data

Variant related genes	Relation type
TMEM135	TF binding region
ENSG00000254843	TF binding region
TMEM135	CpG island
ENSG00000254843	CpG island
ENSG00000174804	chromatin interactions
ENSG00000166575	chromatin interactions
ENSG00000246523	chromatin interactions
ENSG00000254843	chromatin interactions

Extended variants
information (count: 3989 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:3989 , 50 per page) page: 1 2 3 4 5 6 7 ... 80

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs965467	chr11:86776992-86776993	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs12273779	chr11:86777044-86777045	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs77349411	chr11:86777046-86777047	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs181924127	chr11:86777052-86777053	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs965466	chr11:86777067-86777068	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs2512362	chr11:86777114-86777115	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs558110400	chr11:86777123-86777124	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs536199379	chr11:86777133-86777134	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs145966589	chr11:86777161-86777162	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs554173309	chr11:86777209-86777210	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs551285442	chr11:86777223-86777224	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs373180959	chr11:86777247-86777248	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs569241123	chr11:86777274-86777275	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs184897519	chr11:86777317-86777318	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs539401031	chr11:86777375-86777376	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs78583405	chr11:86777440-86777441	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs561741678	chr11:86777450-86777451	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs35075533	chr11:86777511-86777512	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs530602063	chr11:86777531-86777532	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs117515841	chr11:86777565-86777566	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs564097634	chr11:86777591-86777592	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs532833900	chr11:86777624-86777625	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs202228550	chr11:86777641-86777642	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs571906738	chr11:86777658-86777659	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs546824108	chr11:86777716-86777717	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs189223799	chr11:86777749-86777750	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs529020720	chr11:86777769-86777770	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs548786548	chr11:86777821-86777822	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs200116730	chr11:86777824-86777825	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs200397619	chr11:86777825-86777826	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs538319731	chr11:86777833-86777834	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs76188554	chr11:86777840-86777841	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs139843784	chr11:86777848-86777849	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs571571805	chr11:86777881-86777882	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs533951367	chr11:86777908-86777909	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs181655276	chr11:86777958-86777959	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs3133317	chr11:86777967-86777968	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs58096622	chr11:86777980-86777981	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs543373404	chr11:86777983-86777984	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs556781635	chr11:86777992-86777993	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs150659711	chr11:86778041-86778042	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs544290137	chr11:86778073-86778074	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs370102509	chr11:86778097-86778098	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs11234941	chr11:86778113-86778114	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs186865648	chr11:86778114-86778115	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs377451502	chr11:86778116-86778117	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs573492309	chr11:86778150-86778151	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs191256413	chr11:86778183-86778184	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs375554127	chr11:86778207-86778208	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs181124868	chr11:86778266-86778267	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:75)

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
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17157792	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	21364760	CNVD
Ovarian neoplasms	16753589	CNVD
Breast cancer	16608533	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Sudden cardiac death	19188705	CNVD
Prostate cancer	16573809	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
Acute lymphoblastic leukemia	18458336	CNVD
Ductal carcinoma	22052326	CNVD
small cell lung cancer	20016488	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Attention deficit hyperactivity disorder	22241247	CNVD
Breast cancer	21958427	CNVD
Breast cancer	17133270	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Obesity	20622171	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1248 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:86750800-86780600	Weak transcription	Primary T helper cells fromperipheralblood	blood
2	chr11:86750800-86782000	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr11:86750800-86787400	Weak transcription	A549	lung
4	chr11:86751000-86786800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr11:86751000-86787400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr11:86751200-86785600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr11:86751400-86786400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr11:86751600-86787000	Weak transcription	Aorta	Aorta
9	chr11:86755200-86779000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr11:86755400-86780200	Weak transcription	Adipose Nuclei	Adipose
11	chr11:86755400-86780400	Weak transcription	Primary T cells fromperipheralblood	blood
12	chr11:86756400-86782800	Weak transcription	Fetal Intestine Small	intestine
13	chr11:86758200-86778600	Weak transcription	K562	blood
14	chr11:86758200-86780000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
15	chr11:86758200-86780400	Weak transcription	Fetal Muscle Leg	muscle
16	chr11:86758200-86783200	Weak transcription	Primary T cells from cord blood	blood
17	chr11:86758200-86786400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr11:86758400-86778800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr11:86767400-86779000	Weak transcription	HUES64 Cell Line	embryonic stem cell
20	chr11:86767800-86782800	Weak transcription	Left Ventricle	heart
21	chr11:86769000-86786400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr11:86769200-86786400	Weak transcription	Brain Cingulate Gyrus	brain
23	chr11:86769200-86786800	Weak transcription	Brain Anterior Caudate	brain
24	chr11:86769200-86791200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr11:86769200-86792400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
26	chr11:86769400-86778600	Weak transcription	Liver	Liver
27	chr11:86769600-86784800	Weak transcription	Ovary	ovary
28	chr11:86769600-86786600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr11:86770200-86784200	Weak transcription	Duodenum Smooth Muscle	Duodenum
30	chr11:86770400-86808200	Weak transcription	HUVEC	blood vessel
31	chr11:86771000-86786600	Weak transcription	Fetal Brain Male	brain
32	chr11:86771200-86786800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr11:86771400-86778800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr11:86771800-86786000	Weak transcription	Fetal Lung	lung
35	chr11:86773000-86778800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr11:86773000-86783000	Weak transcription	NHDF-Ad	bronchial
37	chr11:86773000-86790800	Weak transcription	NHLF	lung
38	chr11:86773000-86792000	Weak transcription	Primary T helper cells PMA-I stimulated	--
39	chr11:86774200-86782800	Weak transcription	Fetal Stomach	stomach
40	chr11:86774600-86792400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
41	chr11:86774800-86786400	Weak transcription	Lung	lung
42	chr11:86774800-86786800	Weak transcription	Pancreas	Pancrea
43	chr11:86774800-86786800	Weak transcription	Right Ventricle	heart
44	chr11:86774800-86787600	Weak transcription	NHEK	skin
45	chr11:86774800-86806400	Weak transcription	Small Intestine	intestine
46	chr11:86775000-86778600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr11:86775000-86786600	Weak transcription	Colon Smooth Muscle	Colon
48	chr11:86775200-86780400	Weak transcription	HepG2	liver
49	chr11:86775600-86786400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr11:86775600-86791400	Weak transcription	HSMM	muscle

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