Variant report

Variant	nsv1031583
Chromosome Location	chr7:5889011-5970922
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1031)
CpG islands
(count:1344)
Chromatin interactive
region (count:3)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1031 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:5908686-5908892	HepG2	liver:	n/a	n/a
2	BATF	chr7:5938176-5938390	GM12878	blood:	n/a	n/a
3	BATF	chr7:5938735-5938983	GM12878	blood:	n/a	n/a
4	BATF	chr7:5896136-5896348	GM12878	blood:	n/a	n/a
5	BCL11A	chr7:5938179-5938410	GM12878	blood:	n/a	n/a
6	BCL11A	chr7:5938072-5938321	GM12878	blood:	n/a	n/a
7	BCLAF1	chr7:5896165-5896407	GM12878	blood:	n/a	n/a
8	BHLHE40	chr7:5938233-5938412	K562	blood:	n/a	n/a
9	BHLHE40	chr7:5896140-5896326	GM12878	blood:	n/a	n/a
10	BHLHE40	chr7:5889190-5889204	K562	blood:	n/a	n/a
11	BRCA1	chr7:5938138-5938423	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr7:5896176-5896337	Hela-S3	cervix:	n/a	n/a
13	CBX3	chr7:5938925-5939374	K562	blood:	n/a	n/a
14	CBX3	chr7:5937356-5938688	K562	blood:	n/a	n/a
15	CBX3	chr7:5938092-5938432	K562	blood:	n/a	n/a
16	CEBPB	chr7:5890492-5890732	K562	blood:	n/a	chr7:5890571-5890582
17	CEBPB	chr7:5890537-5890656	IMR90	lung:	n/a	chr7:5890571-5890582
18	CEBPB	chr7:5892913-5893127	H1-hESC	embryonic stem cell:	n/a	chr7:5893027-5893038
19	CEBPB	chr7:5890537-5890700	A549	lung:	n/a	chr7:5890571-5890582
20	CEBPB	chr7:5890460-5890688	HepG2	liver:	n/a	chr7:5890571-5890582
21	CEBPB	chr7:5890535-5890604	H1-hESC	embryonic stem cell:	n/a	chr7:5890571-5890582
22	CEBPB	chr7:5942532-5942815	K562	blood:	n/a	chr7:5942734-5942743 chr7:5942734-5942745
23	CEBPB	chr7:5893018-5893091	Hela-S3	cervix:	n/a	chr7:5893027-5893038
24	CEBPB	chr7:5892975-5893174	A549	lung:	n/a	chr7:5893027-5893038
25	CEBPB	chr7:5891846-5891857	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr7:5892975-5893180	HepG2	liver:	n/a	chr7:5893027-5893038
27	CEBPB	chr7:5912087-5912368	IMR90	lung:	n/a	n/a
28	CEBPB	chr7:5929312-5929450	IMR90	lung:	n/a	n/a
29	CEBPB	chr7:5896180-5896389	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr7:5891809-5891870	IMR90	lung:	n/a	n/a
31	CEBPB	chr7:5929893-5930182	K562	blood:	n/a	n/a
32	CEBPB	chr7:5892977-5893179	IMR90	lung:	n/a	chr7:5893027-5893038
33	CEBPB	chr7:5892955-5893172	K562	blood:	n/a	chr7:5893027-5893038
34	CHD2	chr7:5894459-5894465	HepG2	liver:	n/a	n/a
35	CHD2	chr7:5938146-5938417	Hela-S3	cervix:	n/a	n/a
36	CREB1	chr7:5938052-5938355	HepG2	liver:	n/a	n/a
37	CREB1	chr7:5938058-5938399	A549	lung:	n/a	n/a
38	CTCF	chr7:5896200-5896350	GM12864	blood:	n/a	n/a
39	CTCF	chr7:5959212-5959240	GM13976	blood:	n/a	n/a
40	CTCF	chr7:5938160-5938310	NHEK	skin:	n/a	chr7:5938264-5938273
41	CTCF	chr7:5938171-5938382	Hela-S3	cervix:	n/a	chr7:5938264-5938273
42	CTCF	chr7:5896100-5896250	HMF	breast:	n/a	n/a
43	CTCF	chr7:5942920-5943070	Hela-S3	cervix:	n/a	n/a
44	CTCF	chr7:5939088-5939128	MCF-7	breast:	n/a	n/a
45	CTCF	chr7:5938160-5938310	MCF-7	breast:	n/a	chr7:5938264-5938273
46	CTCF	chr7:5937986-5938565	K562	blood:	n/a	chr7:5938264-5938273
47	CTCF	chr7:5896200-5896350	HUVEC	blood vessel:	n/a	n/a
48	CTCF	chr7:5938149-5938390	GM19240	blood:	n/a	chr7:5938264-5938273
49	CTCF	chr7:5938140-5938361	MCF-7	breast:	n/a	chr7:5938264-5938273
50	CTCF	chr7:5896140-5896290	GM06990	blood:	n/a	n/a

(count:1344 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:5890037-5890087	HEK293	kidney:	embryo
2	chr7:5919583-5919633	Jurkat	blood:	n/a
3	chr7:5890037-5890087	HEK293	kidney:	embryo
4	chr7:5919583-5919633	Jurkat	blood:	n/a
5	chr7:5919012-5919062	PrEC	prostate:	n/a
6	chr7:5935002-5935052	PANC-1	pancreas:	n/a
7	chr7:5938193-5938243	AG04449	skin:	fetal
8	chr7:5939791-5939841	NHBE	bronchial:	n/a
9	chr7:5937190-5937240	Hepatocyte	liver:	n/a
10	chr7:5941157-5941207	A549	lung:	n/a
11	chr7:5911701-5911751	HepG2	liver:	n/a
12	chr7:5919012-5919062	U87	brain:	n/a
13	chr7:5935002-5935052	GM12892	blood:	n/a
14	chr7:5937190-5937240	AG10803	skin:	n/a
15	chr7:5919589-5919639	NH-A	brain:	n/a
16	chr7:5937486-5937536	MCF-7	breast:	n/a
17	chr7:5937433-5937483	AG09309	skin:	n/a
18	chr7:5911900-5911950	AG04449	skin:	fetal
19	chr7:5919589-5919639	HCF	heart:	n/a
20	chr7:5920635-5920685	PFSK-1	brain:	n/a
21	chr7:5938227-5938277	GM12891	blood:	n/a
22	chr7:5938227-5938277	BE2_C	brain:	n/a
23	chr7:5920535-5920585	HIPEpiC	eye:	n/a
24	chr7:5938227-5938277	HRE	kidney:	n/a
25	chr7:5938293-5938343	RPTEC	kidney:	n/a
26	chr7:5935002-5935052	Hela-S3	cervix:	n/a
27	chr7:5938227-5938277	HIPEpiC	eye:	n/a
28	chr7:5938288-5938338	Jurkat	blood:	n/a
29	chr7:5938293-5938343	HMEC	breast:	n/a
30	chr7:5937486-5937536	HCF	heart:	n/a
31	chr7:5911800-5911850	MCF10A-Er-Src	breast:	n/a
32	chr7:5919012-5919062	HNPCEpiC	eye:	n/a
33	chr7:5939791-5939841	CMK	blood:	n/a
34	chr7:5937190-5937240	HIPEpiC	eye:	n/a
35	chr7:5935002-5935052	T-47D	breast:	n/a
36	chr7:5919012-5919062	MCF10A-Er-Src	breast:	n/a
37	chr7:5938204-5938254	SK-N-SH	brain:	n/a
38	chr7:5919583-5919633	NHBE	bronchial:	n/a
39	chr7:5938193-5938243	HCT-116	colon:	n/a
40	chr7:5937190-5937240	Hela-S3	cervix:	n/a
41	chr7:5937190-5937240	PFSK-1	brain:	n/a
42	chr7:5938227-5938277	A549	lung:	n/a
43	chr7:5937190-5937240	HCM	heart:	n/a
44	chr7:5919583-5919633	MCF10A-Er-Src	breast:	n/a
45	chr7:5937433-5937483	AG04450	lung:	fetal
46	chr7:5938288-5938338	SK-N-SH	brain:	n/a
47	chr7:5941157-5941207	PFSK-1	brain:	n/a
48	chr7:5938293-5938343	AG09319	gingival:	n/a
49	chr7:5920635-5920685	HUVEC	blood vessel:	n/a
50	chr7:5938227-5938277	HEEpiC	esophagus:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr7:5921888..5923776-chr7:6615172..6617060,2	K562	blood:
2	chr7:5895754..5896691-chr7:6036473..6037181,2	MCF-7	breast:
3	chr7:5896217..5898583-chr7:97641356..97642858,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OCM-2	chr7:5964372-5964445	NONHSAT118958
2	lnc-OCM-2	chr7:5965263-5965571	NONHSAT118958
3	lnc-RSPH10B-1	chr7:5911384-5911681	NONHSAT118956
4	lnc-OCM-3	chr7:5893738-5893857	NONHSAT118944

No data

Variant related genes	Relation type
CCZ1	TF binding region
OCM	TF binding region
RN7SL556P	TF binding region
CCZ1	CpG island
OCM	CpG island
RN7SL556P	CpG island

Extended variants
information (count: 4345 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:4345 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs552821537	chr7:5889021-5889022	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs571034765	chr7:5889037-5889038	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs538759059	chr7:5889038-5889039	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs184099796	chr7:5889051-5889052	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs575242632	chr7:5889068-5889069	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs116880020	chr7:5889115-5889116	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
7	rs554100338	chr7:5889121-5889122	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs308079	chr7:5889126-5889127	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs10807953	chr7:5889147-5889148	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs117674710	chr7:5889172-5889173	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
11	rs6949256	chr7:5889175-5889176	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs11976637	chr7:5889183-5889184	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs77543997	chr7:5889188-5889189	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
14	rs139236800	chr7:5889192-5889193	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs548611802	chr7:5889247-5889248	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs144050055	chr7:5889248-5889249	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs528014286	chr7:5889254-5889255	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs552887213	chr7:5889256-5889257	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs571094652	chr7:5889268-5889269	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs557513207	chr7:5889285-5889286	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs146833341	chr7:5889295-5889296	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs115489396	chr7:5889299-5889300	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs186967516	chr7:5889308-5889309	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs146733003	chr7:5889313-5889314	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs201319030	chr7:5889319-5889320	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs140669407	chr7:5889328-5889329	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs191511249	chr7:5889372-5889373	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs201415359	chr7:5889375-5889376	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs368441792	chr7:5889383-5889384	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs561671509	chr7:5889393-5889394	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs528860862	chr7:5889433-5889434	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs143814497	chr7:5889444-5889445	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs199709158	chr7:5889463-5889464	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs200714212	chr7:5889465-5889466	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs10677628	chr7:5889466-5889467	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs201537211	chr7:5889467-5889468	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs55780043	chr7:5889472-5889473	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs577016773	chr7:5889487-5889488	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs544081753	chr7:5889492-5889493	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs75756274	chr7:5889495-5889496	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
41	rs115445411	chr7:5889497-5889498	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs568929460	chr7:5889501-5889502	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs560504267	chr7:5889522-5889523	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs527676201	chr7:5889529-5889530	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs183630498	chr7:5889543-5889544	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs564627351	chr7:5889551-5889552	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs531988801	chr7:5889576-5889577	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs550120466	chr7:5889604-5889605	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs568609316	chr7:5889621-5889622	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs529765345	chr7:5889623-5889624	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Developmental delay	21147756	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Urothelial carcinoma	21177765	CNVD
Bladder cancer	21909424	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21045282	CNVD
Disorders of sex development	21048976	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Schizophrenia	21346763	CNVD
Acute myeloid leukemia	21251322	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:909 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:5863600-5896800	Weak transcription	Esophagus	oesophagus
2	chr7:5863800-5891400	Weak transcription	Liver	Liver
3	chr7:5863800-5891400	Weak transcription	Brain Hippocampus Middle	brain
4	chr7:5863800-5896200	Weak transcription	Adipose Nuclei	Adipose
5	chr7:5864200-5893600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr7:5871400-5890600	Weak transcription	Brain Germinal Matrix	brain
7	chr7:5871400-5904600	Weak transcription	Spleen	Spleen
8	chr7:5871600-5889200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr7:5871600-5891800	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr7:5871600-5896400	Weak transcription	Fetal Brain Female	brain
11	chr7:5873200-5896200	Weak transcription	Lung	lung
12	chr7:5875400-5896600	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr7:5876400-5896200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
14	chr7:5877400-5896200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
15	chr7:5877600-5891400	Weak transcription	Brain Cingulate Gyrus	brain
16	chr7:5878600-5898000	Weak transcription	Brain Angular Gyrus	brain
17	chr7:5878800-5889600	Strong transcription	Primary neutrophils fromperipheralblood	blood
18	chr7:5882000-5890800	Weak transcription	Fetal Stomach	stomach
19	chr7:5882200-5890800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chr7:5882400-5896000	Weak transcription	Primary B cells from peripheral blood	blood
21	chr7:5882400-5896200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
22	chr7:5882400-5897600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
23	chr7:5882600-5896200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr7:5882800-5896800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
25	chr7:5882800-5896800	Weak transcription	Fetal Intestine Small	intestine
26	chr7:5883000-5897400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
27	chr7:5884400-5889800	Strong transcription	Primary monocytes fromperipheralblood	blood
28	chr7:5885400-5891200	Weak transcription	Brain Anterior Caudate	brain
29	chr7:5887600-5890800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
30	chr7:5887600-5891200	Strong transcription	Primary T cells fromperipheralblood	blood
31	chr7:5887800-5892200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
32	chr7:5887800-5895400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
33	chr7:5888000-5890000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
34	chr7:5888000-5897600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr7:5888400-5889400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr7:5888400-5891400	Strong transcription	Primary T helper cells fromperipheralblood	blood
37	chr7:5888400-5893000	Strong transcription	Primary T cells from cord blood	blood
38	chr7:5888800-5890200	Strong transcription	Primary T helper cells PMA-I stimulated	--
39	chr7:5889000-5889600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
40	chr7:5889000-5889800	Strong transcription	Monocytes-CD14+_RO01746	blood
41	chr7:5889200-5889800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr7:5889400-5890200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr7:5889400-5896000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr7:5889600-5890000	Enhancers	Osteobl	bone
45	chr7:5889600-5895800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
46	chr7:5889600-5896200	Weak transcription	Primary neutrophils fromperipheralblood	blood
47	chr7:5889800-5892000	Weak transcription	Primary monocytes fromperipheralblood	blood
48	chr7:5889800-5892200	Weak transcription	Monocytes-CD14+_RO01746	blood
49	chr7:5889800-5900600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr7:5890000-5924600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood

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