Variant report

Variant	esv33564
Chromosome Location	chr11:92918600-92936545
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:693)
CpG islands
(count:737)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:693 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

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	chr11:92925428-92925626	K562	blood:	n/a	n/a
3	ATF1	chr11:92930464-92930811	K562	blood:	n/a	n/a
4	ATF3	chr11:92930439-92930795	K562	blood:	n/a	n/a
5	BACH1	chr11:92930194-92931093	H1-hESC	embryonic stem cell:	n/a	chr11:92930622-92930636
6	BACH1	chr11:92930348-92930835	K562	blood:	n/a	chr11:92930622-92930636
7	BACH1	chr11:92931235-92931313	K562	blood:	n/a	n/a
8	BATF	chr11:92930451-92930816	GM12878	blood:	n/a	n/a
9	BCLAF1	chr11:92930357-92931221	GM12878	blood:	n/a	chr11:92931040-92931053 chr11:92931044-92931057
10	BCLAF1	chr11:92930350-92931001	GM12878	blood:	n/a	n/a
11	BHLHE40	chr11:92930345-92930997	GM12878	blood:	n/a	n/a
12	BHLHE40	chr11:92930424-92931132	K562	blood:	n/a	chr11:92931043-92931059
13	BHLHE40	chr11:92930474-92931435	HepG2	liver:	n/a	chr11:92931043-92931059
14	BRCA1	chr11:92930149-92931654	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr11:92930869-92931186	HepG2	liver:	n/a	n/a
16	CBX3	chr11:92930416-92931063	K562	blood:	n/a	n/a
17	CCNT2	chr11:92930714-92931265	K562	blood:	n/a	n/a
18	CEBPB	chr11:92931051-92931422	A549	lung:	n/a	n/a
19	CEBPB	chr11:92931003-92931553	A549	lung:	n/a	n/a
20	CEBPB	chr11:92932822-92933072	A549	lung:	n/a	n/a
21	CEBPB	chr11:92931064-92931451	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr11:92931039-92931453	A549	lung:	n/a	n/a
23	CEBPB	chr11:92926904-92927280	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr11:92931084-92931342	HepG2	liver:	n/a	n/a
25	CEBPB	chr11:92931063-92931432	K562	blood:	n/a	n/a
26	CEBPB	chr11:92930453-92931433	IMR90	lung:	n/a	n/a
27	CEBPB	chr11:92931053-92931431	K562	blood:	n/a	n/a
28	CEBPB	chr11:92930552-92930793	K562	blood:	n/a	n/a
29	CEBPB	chr11:92930611-92931454	HepG2	liver:	n/a	n/a
30	CEBPB	chr11:92926914-92927273	HepG2	liver:	n/a	n/a
31	CEBPB	chr11:92930607-92931450	HepG2	liver:	n/a	n/a
32	CEBPB	chr11:92926853-92927287	A549	lung:	n/a	n/a
33	CEBPB	chr11:92931022-92931443	MCF-7	breast:	n/a	n/a
34	CEBPB	chr11:92926895-92927267	K562	blood:	n/a	n/a
35	CEBPB	chr11:92926906-92927262	A549	lung:	n/a	n/a
36	CEBPB	chr11:92926939-92927228	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr11:92926904-92927274	IMR90	lung:	n/a	n/a
38	CEBPB	chr11:92929971-92931626	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr11:92931021-92931462	HepG2	liver:	n/a	n/a
40	CEBPD	chr11:92931047-92931403	HepG2	liver:	n/a	n/a
41	CEBPD	chr11:92930947-92931319	HepG2	liver:	n/a	n/a
42	CHD1	chr11:92930359-92931037	GM12878	blood:	n/a	n/a
43	CHD1	chr11:92930314-92931112	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD1	chr11:92925561-92925620	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD2	chr11:92925444-92925568	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD2	chr11:92930050-92931415	Hela-S3	cervix:	n/a	chr11:92931142-92931152
47	CHD2	chr11:92930859-92931238	H1-hESC	embryonic stem cell:	n/a	chr11:92931142-92931152
48	CHD2	chr11:92930378-92931176	GM12878	blood:	n/a	chr11:92931142-92931152
49	CHD2	chr11:92930408-92931195	HepG2	liver:	n/a	chr11:92931142-92931152
50	CHD2	chr11:92930549-92931241	K562	blood:	n/a	chr11:92931142-92931152

(count:737 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:92930739-92930789	HepG2	liver:	n/a
2	chr11:92928169-92928219	GM12891	blood:	n/a
3	chr11:92931416-92931466	HCT-116	colon:	n/a
4	chr11:92930739-92930789	Jurkat	blood:	n/a
5	chr11:92930990-92931040	T-47D	breast:	n/a
6	chr11:92930739-92930789	HepG2	liver:	n/a
7	chr11:92928169-92928219	GM12891	blood:	n/a
8	chr11:92931416-92931466	HCT-116	colon:	n/a
9	chr11:92930739-92930789	Jurkat	blood:	n/a
10	chr11:92930990-92931040	T-47D	breast:	n/a
11	chr11:92928169-92928219	HNPCEpiC	eye:	n/a
12	chr11:92930777-92930827	T-47D	breast:	n/a
13	chr11:92925402-92925452	RPTEC	kidney:	n/a
14	chr11:92930990-92931040	HCM	heart:	n/a
15	chr11:92931311-92931361	H1-hESC	embryonic stem cell:	embryo
16	chr11:92931280-92931330	SK-N-SH_RA	brain:	n/a
17	chr11:92931304-92931354	SAEC	small airway:	n/a
18	chr11:92931311-92931361	GM12891	blood:	n/a
19	chr11:92930777-92930827	U87	brain:	n/a
20	chr11:92931304-92931354	Hela-S3	cervix:	n/a
21	chr11:92928169-92928219	GM12892	blood:	n/a
22	chr11:92931416-92931466	HCM	heart:	n/a
23	chr11:92925402-92925452	MCF10A-Er-Src	breast:	n/a
24	chr11:92931304-92931354	HCPEpiC	choroid plexus:	n/a
25	chr11:92928169-92928219	LNCaP	prostate:	n/a
26	chr11:92931311-92931361	HIPEpiC	eye:	n/a
27	chr11:92925402-92925452	A549	lung:	n/a
28	chr11:92931250-92931300	PrEC	prostate:	n/a
29	chr11:92930739-92930789	HEEpiC	esophagus:	n/a
30	chr11:92931304-92931354	HCM	heart:	n/a
31	chr11:92928169-92928219	IMR90	lung:	fetal
32	chr11:92931416-92931466	SK-N-SH_RA	brain:	n/a
33	chr11:92931390-92931440	GM12891	blood:	n/a
34	chr11:92931304-92931354	ProgFib	skin:	n/a
35	chr11:92930916-92930966	HUVEC	blood vessel:	n/a
36	chr11:92930990-92931040	LNCaP	prostate:	n/a
37	chr11:92930916-92930966	Caco-2	colon:	n/a
38	chr11:92928169-92928219	HUVEC	blood vessel:	n/a
39	chr11:92931390-92931440	BE2_C	brain:	n/a
40	chr11:92930739-92930789	ECC-1	luminal epithelium:	n/a
41	chr11:92930916-92930966	ovcar-3	ovarian:	n/a
42	chr11:92928169-92928219	AG04449	skin:	fetal
43	chr11:92930990-92931040	NB4	blood:	n/a
44	chr11:92931311-92931361	GM12878	blood:	n/a
45	chr11:92925402-92925452	AG09309	skin:	n/a
46	chr11:92925402-92925452	HCF	heart:	n/a
47	chr11:92931390-92931440	LNCaP	prostate:	n/a
48	chr11:92925402-92925452	NHBE	bronchial:	n/a
49	chr11:92931250-92931300	LNCaP	prostate:	n/a
50	chr11:92931390-92931440	SK-N-SH	brain:	n/a

(count:18 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 533 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:533 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs34733694	chr11:92918673-92918674	Weak transcription ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs74810885	chr11:92918689-92918690	Weak transcription ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs376887900	chr11:92918700-92918701	Weak transcription ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs559357716	chr11:92918716-92918717	Weak transcription ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs558621212	chr11:92918722-92918723	Weak transcription ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs530295972	chr11:92918765-92918766	Weak transcription ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs576821473	chr11:92918869-92918870	Weak transcription ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs149765900	chr11:92918884-92918885	Weak transcription ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs145733130	chr11:92918908-92918909	Weak transcription ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs544433678	chr11:92918964-92918965	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs190202644	chr11:92918967-92918968	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs35902979	chr11:92919042-92919043	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs34259595	chr11:92919049-92919050	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs16918635	chr11:92919058-92919059	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs574810255	chr11:92919067-92919068	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs114288487	chr11:92919122-92919123	Weak transcription ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs550601237	chr11:92919176-92919177	Weak transcription ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs570345592	chr11:92919231-92919232	Weak transcription ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs143517520	chr11:92919298-92919299	Weak transcription ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs147152957	chr11:92919306-92919307	Weak transcription ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs183413413	chr11:92919344-92919345	Weak transcription ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs564615578	chr11:92919368-92919369	Weak transcription ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs187489603	chr11:92919383-92919384	Weak transcription ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs550396651	chr11:92919423-92919424	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs568292820	chr11:92919444-92919445	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs529412690	chr11:92919447-92919448	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs547705502	chr11:92919485-92919486	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs565985484	chr11:92919501-92919502	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs74753544	chr11:92919551-92919552	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs192760421	chr11:92919593-92919594	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs184529528	chr11:92919594-92919595	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs537518544	chr11:92919600-92919601	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs574307632	chr11:92919649-92919650	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs556434514	chr11:92919660-92919661	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs548883635	chr11:92919676-92919677	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs574703557	chr11:92919724-92919725	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs187802981	chr11:92919778-92919779	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs575017842	chr11:92919808-92919809	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs570102617	chr11:92919888-92919889	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs572207588	chr11:92919910-92919911	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs369329546	chr11:92919911-92919912	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs546220183	chr11:92920034-92920035	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs192674873	chr11:92920072-92920073	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs76594445	chr11:92920100-92920101	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs140272824	chr11:92920115-92920116	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs184327660	chr11:92920124-92920125	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs575694521	chr11:92920143-92920144	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs529448081	chr11:92920173-92920174	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs547543628	chr11:92920176-92920177	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs559658949	chr11:92920298-92920299	Weak transcription ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:77)

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

Chromatin state (count:636 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:92891600-92925400	Weak transcription	Fetal Heart	heart
2	chr11:92891800-92929800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
3	chr11:92895400-92920000	Weak transcription	Psoas Muscle	Psoas
4	chr11:92895400-92921400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr11:92898200-92919800	Weak transcription	Brain Angular Gyrus	brain
6	chr11:92898200-92920000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
7	chr11:92900600-92929600	Weak transcription	HUVEC	blood vessel
8	chr11:92910800-92918600	Weak transcription	Fetal Kidney	kidney
9	chr11:92911200-92930000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr11:92911400-92919000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr11:92911400-92919200	Weak transcription	Fetal Intestine Small	intestine
12	chr11:92911400-92925400	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr11:92911600-92918800	Strong transcription	Primary monocytes fromperipheralblood	blood
14	chr11:92911600-92919600	Weak transcription	Brain Inferior Temporal Lobe	brain
15	chr11:92911600-92920000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr11:92911600-92920000	Weak transcription	HMEC	breast
17	chr11:92911600-92920000	Weak transcription	HSMMtube	muscle
18	chr11:92911600-92920800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
19	chr11:92911600-92925400	Weak transcription	Esophagus	oesophagus
20	chr11:92911600-92925400	Weak transcription	Gastric	stomach
21	chr11:92911600-92929800	Weak transcription	Right Ventricle	heart
22	chr11:92911600-92930000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr11:92911800-92920000	Weak transcription	Placenta	Placenta
24	chr11:92911800-92929800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr11:92911800-92930200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr11:92912200-92920200	Weak transcription	Stomach Smooth Muscle	stomach
27	chr11:92912200-92920800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr11:92912200-92929800	Weak transcription	Rectal Smooth Muscle	rectum
29	chr11:92912200-92929800	Weak transcription	Thymus	Thymus
30	chr11:92912200-92930000	Weak transcription	Fetal Stomach	stomach
31	chr11:92912400-92919000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr11:92912400-92919000	Weak transcription	Brain Anterior Caudate	brain
33	chr11:92912400-92920200	Weak transcription	HepG2	liver
34	chr11:92912400-92920600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
35	chr11:92912400-92929800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
36	chr11:92912400-92930000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr11:92912600-92918800	Strong transcription	Primary hematopoietic stem cells	blood
38	chr11:92912600-92919200	Strong transcription	HUES48 Cell Line	embryonic stem cell
39	chr11:92912600-92919800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr11:92912600-92919800	Weak transcription	Skeletal Muscle Female	skeletal muscle
41	chr11:92912600-92920600	Weak transcription	Rectal Mucosa Donor 31	rectum
42	chr11:92912600-92920800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr11:92912600-92920800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
44	chr11:92912600-92920800	Weak transcription	Left Ventricle	heart
45	chr11:92912600-92921000	Weak transcription	Ovary	ovary
46	chr11:92912600-92923000	Weak transcription	Colon Smooth Muscle	Colon
47	chr11:92912600-92924000	Weak transcription	Placenta Amnion	Placenta Amnion
48	chr11:92912600-92926800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
49	chr11:92912600-92928000	Weak transcription	Sigmoid Colon	Sigmoid Colon
50	chr11:92912800-92919000	Strong transcription	Monocytes-CD14+_RO01746	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links