Variant report

Variant	nsv1039908
Chromosome Location	chr11:120904893-120936907
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:303)
CpG islands
(count:122)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:303 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:120934411-120934811	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:120909466-120910036	HepG2	liver:	n/a	n/a
3	ATF2	chr11:120906519-120907016	GM12878	blood:	n/a	n/a
4	ATF2	chr11:120930349-120930746	GM12878	blood:	n/a	n/a
5	BATF	chr11:120930369-120930615	GM12878	blood:	n/a	n/a
6	BATF	chr11:120930372-120930584	GM12878	blood:	n/a	n/a
7	BHLHE40	chr11:120909753-120910121	HepG2	liver:	n/a	n/a
8	BHLHE40	chr11:120930352-120930657	GM12878	blood:	n/a	n/a
9	BHLHE40	chr11:120906525-120906898	GM12878	blood:	n/a	n/a
10	CEBPB	chr11:120928570-120928864	K562	blood:	n/a	n/a
11	CEBPB	chr11:120928580-120928888	A549	lung:	n/a	n/a
12	CEBPB	chr11:120921803-120922083	HepG2	liver:	n/a	n/a
13	CEBPB	chr11:120928540-120928906	IMR90	lung:	n/a	n/a
14	CEBPB	chr11:120928567-120928905	HepG2	liver:	n/a	n/a
15	CHD1	chr11:120929538-120929839	GM12878	blood:	n/a	n/a
16	CHD2	chr11:120930396-120930841	GM12878	blood:	n/a	n/a
17	CTCF	chr11:120934580-120934730	BJ	skin:	n/a	n/a
18	CTCF	chr11:120934700-120934850	RPTEC	kidney:	n/a	n/a
19	CTCF	chr11:120934580-120934730	GM12869	blood:	n/a	n/a
20	CTCF	chr11:120934560-120934710	AG04449	skin:	n/a	n/a
21	CTCF	chr11:120934560-120934710	HEEpiC	esophagus:	n/a	n/a
22	CTCF	chr11:120934600-120934750	AG09309	skin:	n/a	n/a
23	CTCF	chr11:120934500-120934650	NB4	blood:	n/a	n/a
24	CTCF	chr11:120934566-120934697	Hela-S3	cervix:	n/a	n/a
25	CTCF	chr11:120934600-120934750	HFF-Myc	foreskin:	n/a	n/a
26	CTCF	chr11:120934840-120934990	BJ	skin:	n/a	chr11:120934898-120934919
27	CTCF	chr11:120934560-120934710	MCF-7	breast:	n/a	n/a
28	CTCF	chr11:120934560-120934710	AG10803	skin:	n/a	n/a
29	CTCF	chr11:120934640-120934790	GM12873	blood:	n/a	n/a
30	CTCF	chr11:120936480-120936630	BJ	skin:	n/a	n/a
31	CTCF	chr11:120934540-120934690	HUVEC	blood vessel:	n/a	n/a
32	CTCF	chr11:120934540-120934690	HPF	lung:	n/a	n/a
33	CTCF	chr11:120934540-120934690	GM12868	blood:	n/a	n/a
34	CTCF	chr11:120934480-120934630	GM12872	blood:	n/a	n/a
35	CTCF	chr11:120934560-120934710	GM12866	blood:	n/a	n/a
36	CTCF	chr11:120934500-120934650	HCM	heart:	n/a	n/a
37	CTCF	chr11:120934580-120934730	HRPEpiC	eye:	n/a	n/a
38	CTCF	chr11:120934520-120934670	GM12872	blood:	n/a	n/a
39	CTCF	chr11:120934560-120934710	HL-60	blood:	n/a	n/a
40	CTCF	chr11:120934500-120934650	WERI-Rb-1	eye:	n/a	n/a
41	CTCF	chr11:120934520-120934670	AG09309	skin:	n/a	n/a
42	CTCF	chr11:120934700-120934850	HCM	heart:	n/a	n/a
43	CTCF	chr11:120934580-120934730	HEEpiC	esophagus:	n/a	n/a
44	CTCF	chr11:120934567-120934718	K562	blood:	n/a	n/a
45	CTCF	chr11:120934560-120934710	A549	lung:	n/a	n/a
46	CTCF	chr11:120934560-120934710	GM12874	blood:	n/a	n/a
47	CTCF	chr11:120934600-120934750	NHLF	lung:	n/a	n/a
48	CTCF	chr11:120917920-120918070	NHEK	skin:	n/a	n/a
49	CTCF	chr11:120917960-120918110	GM12868	blood:	n/a	n/a
50	CTCF	chr11:120934620-120934770	BJ	skin:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:120933166-120933216	GM06990	blood:	n/a
2	chr11:120911604-120911654	GM12892	blood:	n/a
3	chr11:120933166-120933216	HAEpiC	amniotic membrane:	n/a
4	chr11:120911604-120911654	GM19239	blood:	n/a
5	chr11:120911604-120911654	NHDF-neo	bronchial:	n/a
6	chr11:120933166-120933216	HCT-116	colon:	n/a
7	chr11:120933166-120933216	SK-N-SH	brain:	n/a
8	chr11:120933166-120933216	Hela-S3	cervix:	n/a
9	chr11:120933166-120933216	MCF-7	breast:	n/a
10	chr11:120911604-120911654	HIPEpiC	eye:	n/a
11	chr11:120933166-120933216	HCPEpiC	choroid plexus:	n/a
12	chr11:120911604-120911654	HRCEpiC	kidney:	n/a
13	chr11:120911604-120911654	AG04449	skin:	fetal
14	chr11:120933166-120933216	NH-A	brain:	n/a
15	chr11:120933166-120933216	LNCaP	prostate:	n/a
16	chr11:120933166-120933216	NB4	blood:	n/a
17	chr11:120933166-120933216	RPTEC	kidney:	n/a
18	chr11:120933166-120933216	Jurkat	blood:	n/a
19	chr11:120933166-120933216	AG04450	lung:	fetal
20	chr11:120911604-120911654	HAEpiC	amniotic membrane:	n/a
21	chr11:120911604-120911654	U87	brain:	n/a
22	chr11:120911604-120911654	AG09309	skin:	n/a
23	chr11:120911604-120911654	NB4	blood:	n/a
24	chr11:120911604-120911654	SKMC	muscle:	n/a
25	chr11:120933166-120933216	AG09309	skin:	n/a
26	chr11:120911604-120911654	Caco-2	colon:	n/a
27	chr11:120911604-120911654	Hela-S3	cervix:	n/a
28	chr11:120911604-120911654	T-47D	breast:	n/a
29	chr11:120911604-120911654	HCM	heart:	n/a
30	chr11:120911604-120911654	SAEC	small airway:	n/a
31	chr11:120933166-120933216	AoSMC	blood vessel:	n/a
32	chr11:120911604-120911654	BE2_C	brain:	n/a
33	chr11:120911604-120911654	GM12891	blood:	n/a
34	chr11:120911604-120911654	IMR90	lung:	fetal
35	chr11:120911604-120911654	HCPEpiC	choroid plexus:	n/a
36	chr11:120933166-120933216	GM12891	blood:	n/a
37	chr11:120933166-120933216	HL-60	blood:	n/a
38	chr11:120933166-120933216	BE2_C	brain:	n/a
39	chr11:120933166-120933216	BJ	skin:	n/a
40	chr11:120911604-120911654	RPTEC	kidney:	n/a
41	chr11:120933166-120933216	Hepatocyte	liver:	n/a
42	chr11:120911604-120911654	HepG2	liver:	n/a
43	chr11:120933166-120933216	PrEC	prostate:	n/a
44	chr11:120911604-120911654	PANC-1	pancreas:	n/a
45	chr11:120911604-120911654	HCT-116	colon:	n/a
46	chr11:120933166-120933216	ovcar-3	ovarian:	n/a
47	chr11:120911604-120911654	HRE	kidney:	n/a
48	chr11:120933166-120933216	NHDF-neo	bronchial:	n/a
49	chr11:120911604-120911654	SK-N-MC	brain:	n/a
50	chr11:120933166-120933216	AG10803	skin:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:120933457..120936231-chr11:120943886..120945409,2	MCF-7	breast:
2	chr11:120909945..120911448-chr11:120913207..120914723,2	MCF-7	breast:
3	chr11:120909945..120911448-chr11:120913207..120914723,2	MCF-7	breast:

No data

Variant related genes	Relation type
TBCEL	TF binding region
TBCEL	CpG island

Extended variants
information (count: 1117 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:1117 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs73589520	chr11:120904930-120904931	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs576513245	chr11:120904978-120904979	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs544038386	chr11:120905024-120905025	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs192823834	chr11:120905028-120905029	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs185858952	chr11:120905032-120905033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs541573605	chr11:120905140-120905141	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs559478682	chr11:120905159-120905160	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs533412180	chr11:120905180-120905181	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs111689042	chr11:120905200-120905201	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs564418178	chr11:120905231-120905232	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs7934730	chr11:120905232-120905233	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs549589437	chr11:120905288-120905289	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs190384050	chr11:120905309-120905310	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs535161413	chr11:120905404-120905405	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs559032789	chr11:120905411-120905412	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs78900013	chr11:120905437-120905438	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs565534247	chr11:120905531-120905532	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs142769294	chr11:120905535-120905536	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs538277031	chr11:120905550-120905551	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs11601464	chr11:120905551-120905552	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs181014430	chr11:120905576-120905577	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs150738894	chr11:120905577-120905578	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs183732026	chr11:120905604-120905605	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs544511016	chr11:120905665-120905666	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs555981980	chr11:120905739-120905740	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs139077384	chr11:120905752-120905753	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs74801699	chr11:120905755-120905756	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs2000526	chr11:120905771-120905772	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs577921376	chr11:120905779-120905780	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs375520724	chr11:120905799-120905800	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs188143422	chr11:120905800-120905801	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs149934992	chr11:120905805-120905806	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs181341266	chr11:120905806-120905807	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs12803528	chr11:120905810-120905811	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs73011552	chr11:120905887-120905888	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs11605695	chr11:120905974-120905975	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs376686361	chr11:120906075-120906076	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs370707111	chr11:120906081-120906082	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs79853313	chr11:120906082-120906083	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs185507199	chr11:120906096-120906097	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs190664291	chr11:120906107-120906108	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs569585324	chr11:120906121-120906122	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs537731908	chr11:120906132-120906133	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs556143213	chr11:120906142-120906143	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs143995385	chr11:120906153-120906154	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs535244665	chr11:120906154-120906155	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs200027443	chr11:120906156-120906157	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs553160481	chr11:120906167-120906168	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs593476	chr11:120906174-120906175	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs578066059	chr11:120906177-120906178	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	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
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	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
Glioblastoma multiforme	21080181	CNVD
Cancer	22429812	CNVD
Breast cancer	16608533	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17603634	CNVD
Breast cancer	21364760	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Ovarian cancer	21720365	CNVD
Neuroblastoma	17327916	CNVD
Malignant melanoma	17260012	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Renal cell carcinoma	21668985	CNVD
Developmental delay	21147756	CNVD
Squamous cell cancer	20885788	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Neurocytoma	17123091	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Central neurocytomas	17123091	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	16750200	CNVD
Multiple myeloma	17550852	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Acute myeloid leukemia	19651601	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	20409316	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Heart disease	20551144	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Autism	22543975	CNVD
Breast cancer	21509527	CNVD
Barrett''s syndrome	19417022	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	21385341	CNVD
Multiple myeloma	16461302	CNVD
Burkitt''s lymphoma	18698080	CNVD
Prostate cancer	23792589	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:749 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:120895800-120918000	Weak transcription	Fetal Muscle Trunk	muscle
2	chr11:120896000-120905600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr11:120896000-120905800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr11:120896000-120910800	Weak transcription	Brain Angular Gyrus	brain
5	chr11:120896000-120910800	Weak transcription	Gastric	stomach
6	chr11:120896000-120915400	Weak transcription	Primary hematopoietic stem cells	blood
7	chr11:120896000-120919600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr11:120896000-120938600	Weak transcription	Lung	lung
9	chr11:120896200-120906400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr11:120896200-120909000	Weak transcription	Fetal Intestine Small	intestine
11	chr11:120896200-120909400	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr11:120896200-120909600	Weak transcription	Small Intestine	intestine
13	chr11:120896200-120913000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
14	chr11:120896200-120916200	Weak transcription	HSMM	muscle
15	chr11:120896200-120916400	Weak transcription	Primary B cells from peripheral blood	blood
16	chr11:120896200-120916600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr11:120896200-120924200	Weak transcription	Rectal Mucosa Donor 31	rectum
18	chr11:120896200-120959600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
19	chr11:120896400-120906200	Weak transcription	HUES48 Cell Line	embryonic stem cell
20	chr11:120896400-120916600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr11:120896400-120917800	Weak transcription	Duodenum Smooth Muscle	Duodenum
22	chr11:120896400-120918000	Weak transcription	Brain Germinal Matrix	brain
23	chr11:120896400-120924400	Weak transcription	Muscle Satellite Cultured Cells	--
24	chr11:120896600-120905600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr11:120896600-120906200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr11:120896600-120906800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr11:120896600-120917200	Weak transcription	Primary T cells fromperipheralblood	blood
28	chr11:120896600-120917600	Weak transcription	Fetal Brain Female	brain
29	chr11:120896600-120917800	Weak transcription	Stomach Smooth Muscle	stomach
30	chr11:120896600-120924000	Weak transcription	Fetal Muscle Leg	muscle
31	chr11:120896600-120938200	Weak transcription	Fetal Stomach	stomach
32	chr11:120896800-120912200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr11:120896800-120917600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
34	chr11:120898800-120906200	Weak transcription	Ovary	ovary
35	chr11:120898800-120938400	Weak transcription	Aorta	Aorta
36	chr11:120899200-120912600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr11:120900800-120917800	Weak transcription	HSMMtube	muscle
38	chr11:120900800-120949800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
39	chr11:120901000-120906200	Weak transcription	Fetal Lung	lung
40	chr11:120901000-120910800	Weak transcription	Psoas Muscle	Psoas
41	chr11:120901000-120917600	Weak transcription	Primary T helper cells PMA-I stimulated	--
42	chr11:120901200-120918000	Weak transcription	Left Ventricle	heart
43	chr11:120901400-120915600	Weak transcription	Primary T cells from cord blood	blood
44	chr11:120901400-120924200	Weak transcription	Right Ventricle	heart
45	chr11:120901800-120916400	Weak transcription	Primary B cells from cord blood	blood
46	chr11:120902800-120907800	Enhancers	Liver	Liver
47	chr11:120903600-120905800	Weak transcription	HepG2	liver
48	chr11:120903800-120916400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr11:120904000-120905000	Enhancers	Fetal Intestine Large	intestine
50	chr11:120905000-120906600	Enhancers	Pancreatic Islets	Pancreatic Islet

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