Variant report

Variant	esv2829957
Chromosome Location	chr11:92915544-92932229
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:687)
CpG islands
(count:734)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:687 , 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	chr11:92925428-92925626	K562	blood:	n/a	n/a
2	ARID3A	chr11:92930141-92931015	HepG2	liver:	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	chr11:92931235-92931313	K562	blood:	n/a	n/a
6	BACH1	chr11:92930348-92930835	K562	blood:	n/a	chr11:92930622-92930636
7	BACH1	chr11:92930194-92931093	H1-hESC	embryonic stem cell:	n/a	chr11:92930622-92930636
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	chr11:92930869-92931186	HepG2	liver:	n/a	n/a
15	BRCA1	chr11:92930149-92931654	Hela-S3	cervix:	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	chr11:92931063-92931432	K562	blood:	n/a	n/a
20	CEBPB	chr11:92926904-92927280	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr11:92931053-92931431	K562	blood:	n/a	n/a
22	CEBPB	chr11:92926853-92927287	A549	lung:	n/a	n/a
23	CEBPB	chr11:92931003-92931553	A549	lung:	n/a	n/a
24	CEBPB	chr11:92930611-92931454	HepG2	liver:	n/a	n/a
25	CEBPB	chr11:92931021-92931462	HepG2	liver:	n/a	n/a
26	CEBPB	chr11:92926904-92927274	IMR90	lung:	n/a	n/a
27	CEBPB	chr11:92930607-92931450	HepG2	liver:	n/a	n/a
28	CEBPB	chr11:92926939-92927228	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr11:92931064-92931451	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr11:92930552-92930793	K562	blood:	n/a	n/a
31	CEBPB	chr11:92926906-92927262	A549	lung:	n/a	n/a
32	CEBPB	chr11:92930453-92931433	IMR90	lung:	n/a	n/a
33	CEBPB	chr11:92931039-92931453	A549	lung:	n/a	n/a
34	CEBPB	chr11:92931084-92931342	HepG2	liver:	n/a	n/a
35	CEBPB	chr11:92931022-92931443	MCF-7	breast:	n/a	n/a
36	CEBPB	chr11:92926895-92927267	K562	blood:	n/a	n/a
37	CEBPB	chr11:92929971-92931626	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr11:92926914-92927273	HepG2	liver:	n/a	n/a
39	CEBPD	chr11:92931047-92931403	HepG2	liver:	n/a	n/a
40	CEBPD	chr11:92930947-92931319	HepG2	liver:	n/a	n/a
41	CHD1	chr11:92925561-92925620	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD1	chr11:92930314-92931112	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD1	chr11:92930359-92931037	GM12878	blood:	n/a	n/a
44	CHD2	chr11:92930050-92931415	Hela-S3	cervix:	n/a	chr11:92931142-92931152
45	CHD2	chr11:92930378-92931176	GM12878	blood:	n/a	chr11:92931142-92931152
46	CHD2	chr11:92930408-92931195	HepG2	liver:	n/a	chr11:92931142-92931152
47	CHD2	chr11:92930549-92931241	K562	blood:	n/a	chr11:92931142-92931152
48	CHD2	chr11:92930859-92931238	H1-hESC	embryonic stem cell:	n/a	chr11:92931142-92931152
49	CHD2	chr11:92925444-92925568	H1-hESC	embryonic stem cell:	n/a	n/a
50	CREB1	chr11:92930343-92930990	GM12878	blood:	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	chr11:92931311-92931361	A549	lung:	n/a
2	chr11:92930739-92930789	SAEC	small airway:	n/a
3	chr11:92931311-92931361	A549	lung:	n/a
4	chr11:92930739-92930789	SAEC	small airway:	n/a
5	chr11:92930990-92931040	HAEpiC	amniotic membrane:	n/a
6	chr11:92931416-92931466	GM06990	blood:	n/a
7	chr11:92931416-92931466	HPAEpiC	pulmonary alveolar:	n/a
8	chr11:92931304-92931354	AG04450	lung:	fetal
9	chr11:92931416-92931466	MCF-7	breast:	n/a
10	chr11:92931304-92931354	RPTEC	kidney:	n/a
11	chr11:92930916-92930966	AG09319	gingival:	n/a
12	chr11:92931311-92931361	BE2_C	brain:	n/a
13	chr11:92931311-92931361	AG09309	skin:	n/a
14	chr11:92931250-92931300	NH-A	brain:	n/a
15	chr11:92930990-92931040	BE2_C	brain:	n/a
16	chr11:92930916-92930966	ovcar-3	ovarian:	n/a
17	chr11:92928169-92928219	HepG2	liver:	n/a
18	chr11:92928169-92928219	GM12878	blood:	n/a
19	chr11:92931390-92931440	ovcar-3	ovarian:	n/a
20	chr11:92930990-92931040	HPAEpiC	pulmonary alveolar:	n/a
21	chr11:92931390-92931440	SK-N-SH	brain:	n/a
22	chr11:92928169-92928219	GM06990	blood:	n/a
23	chr11:92931311-92931361	HCT-116	colon:	n/a
24	chr11:92930777-92930827	SAEC	small airway:	n/a
25	chr11:92930777-92930827	H1-hESC	embryonic stem cell:	embryo
26	chr11:92931304-92931354	HPAEpiC	pulmonary alveolar:	n/a
27	chr11:92928169-92928219	ovcar-3	ovarian:	n/a
28	chr11:92931311-92931361	HEEpiC	esophagus:	n/a
29	chr11:92931280-92931330	HMEC	breast:	n/a
30	chr11:92931390-92931440	HPAEpiC	pulmonary alveolar:	n/a
31	chr11:92931250-92931300	AG09319	gingival:	n/a
32	chr11:92931416-92931466	ProgFib	skin:	n/a
33	chr11:92928169-92928219	HCT-116	colon:	n/a
34	chr11:92931311-92931361	HRE	kidney:	n/a
35	chr11:92930916-92930966	K562	blood:	n/a
36	chr11:92931390-92931440	PFSK-1	brain:	n/a
37	chr11:92931280-92931330	NT2-D1	testis:	n/a
38	chr11:92930990-92931040	AG04450	lung:	fetal
39	chr11:92931311-92931361	ECC-1	luminal epithelium:	n/a
40	chr11:92931304-92931354	HEK293	kidney:	embryo
41	chr11:92930916-92930966	MCF10A-Er-Src	breast:	n/a
42	chr11:92931280-92931330	ECC-1	luminal epithelium:	n/a
43	chr11:92930990-92931040	SKMC	muscle:	n/a
44	chr11:92931250-92931300	RPTEC	kidney:	n/a
45	chr11:92931311-92931361	CMK	blood:	n/a
46	chr11:92931250-92931300	Caco-2	colon:	n/a
47	chr11:92930916-92930966	CMK	blood:	n/a
48	chr11:92930990-92931040	HEK293	kidney:	embryo
49	chr11:92931311-92931361	AG04450	lung:	fetal
50	chr11:92925402-92925452	BE2_C	brain:	n/a

(count:15 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 542 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:542 , 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	rs11020190	chr11:92915544-92915545	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs150736710	chr11:92915571-92915572	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs189574483	chr11:92915678-92915679	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs193072807	chr11:92915731-92915732	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs567260941	chr11:92915740-92915741	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs534599297	chr11:92915762-92915763	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs552975894	chr11:92915779-92915780	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs377230376	chr11:92915802-92915803	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs139481747	chr11:92915866-92915867	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs375735563	chr11:92915880-92915881	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs542138186	chr11:92915891-92915892	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs375095822	chr11:92915931-92915932	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs369604664	chr11:92915934-92915935	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs141009557	chr11:92915991-92915992	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs200901654	chr11:92915997-92915998	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs557194595	chr11:92916030-92916031	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs375726895	chr11:92916069-92916070	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs375452321	chr11:92916080-92916081	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs368228352	chr11:92916104-92916105	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs575646571	chr11:92916143-92916144	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs144978717	chr11:92916145-92916146	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs555198017	chr11:92916160-92916161	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs184762651	chr11:92916181-92916182	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs10831001	chr11:92916228-92916229	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs530904102	chr11:92916261-92916262	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs7925273	chr11:92916271-92916272	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs10831002	chr11:92916282-92916283	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs564635953	chr11:92916288-92916289	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs147959599	chr11:92916289-92916290	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs539397578	chr11:92916333-92916334	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs188829087	chr11:92916407-92916408	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs548809062	chr11:92916417-92916418	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs181568219	chr11:92916422-92916423	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs559130193	chr11:92916425-92916426	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs532516341	chr11:92916429-92916430	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs141901855	chr11:92916436-92916437	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs185316894	chr11:92916442-92916443	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs571179813	chr11:92916510-92916511	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs77084489	chr11:92916539-92916540	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs188516844	chr11:92916543-92916544	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs150061261	chr11:92916589-92916590	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs181598555	chr11:92916679-92916680	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs566712892	chr11:92916769-92916770	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs555236874	chr11:92916792-92916793	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs16918625	chr11:92916819-92916820	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs368210823	chr11:92916836-92916837	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs534364335	chr11:92916858-92916859	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs557621293	chr11:92916870-92916871	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs71480667	chr11:92916874-92916875	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs544721525	chr11:92916879-92916880	Weak transcription Strong transcription	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:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

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	chr11:92897800-92917200	Weak transcription	NHDF-Ad	bronchial
6	chr11:92898200-92919800	Weak transcription	Brain Angular Gyrus	brain
7	chr11:92898200-92920000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
8	chr11:92900600-92929600	Weak transcription	HUVEC	blood vessel
9	chr11:92910800-92918600	Weak transcription	Fetal Kidney	kidney
10	chr11:92911200-92930000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr11:92911400-92919000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr11:92911400-92919200	Weak transcription	Fetal Intestine Small	intestine
13	chr11:92911400-92925400	Weak transcription	Skeletal Muscle Male	skeletal muscle
14	chr11:92911600-92918800	Strong transcription	Primary monocytes fromperipheralblood	blood
15	chr11:92911600-92919600	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr11:92911600-92920000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr11:92911600-92920000	Weak transcription	HMEC	breast
18	chr11:92911600-92920000	Weak transcription	HSMMtube	muscle
19	chr11:92911600-92920800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
20	chr11:92911600-92925400	Weak transcription	Esophagus	oesophagus
21	chr11:92911600-92925400	Weak transcription	Gastric	stomach
22	chr11:92911600-92929800	Weak transcription	Right Ventricle	heart
23	chr11:92911600-92930000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr11:92911800-92915800	Weak transcription	Fetal Thymus	thymus
25	chr11:92911800-92920000	Weak transcription	Placenta	Placenta
26	chr11:92911800-92929800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr11:92911800-92930200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr11:92912000-92915800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr11:92912200-92920200	Weak transcription	Stomach Smooth Muscle	stomach
30	chr11:92912200-92920800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr11:92912200-92929800	Weak transcription	Rectal Smooth Muscle	rectum
32	chr11:92912200-92929800	Weak transcription	Thymus	Thymus
33	chr11:92912200-92930000	Weak transcription	Fetal Stomach	stomach
34	chr11:92912400-92917400	Weak transcription	Cortex derived primary cultured neurospheres	brain
35	chr11:92912400-92919000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr11:92912400-92919000	Weak transcription	Brain Anterior Caudate	brain
37	chr11:92912400-92920200	Weak transcription	HepG2	liver
38	chr11:92912400-92920600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
39	chr11:92912400-92929800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
40	chr11:92912400-92930000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr11:92912600-92915800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr11:92912600-92916200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
43	chr11:92912600-92917400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
44	chr11:92912600-92918000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr11:92912600-92918200	Weak transcription	Fetal Brain Male	brain
46	chr11:92912600-92918400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr11:92912600-92918800	Strong transcription	Primary hematopoietic stem cells	blood
48	chr11:92912600-92919200	Strong transcription	HUES48 Cell Line	embryonic stem cell
49	chr11:92912600-92919800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr11:92912600-92919800	Weak transcription	Skeletal Muscle Female	skeletal muscle

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