Variant report

Variant	nsv1027345
Chromosome Location	chr7:5874854-5931883
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:420)
CpG islands
(count:855)
Chromatin interactive
region (count:8)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:420 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

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	chr7:5896136-5896348	GM12878	blood:	n/a	n/a
3	BCLAF1	chr7:5896165-5896407	GM12878	blood:	n/a	n/a
4	BHLHE40	chr7:5889190-5889204	K562	blood:	n/a	n/a
5	BHLHE40	chr7:5896140-5896326	GM12878	blood:	n/a	n/a
6	BRCA1	chr7:5896176-5896337	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr7:5891846-5891857	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr7:5892955-5893172	K562	blood:	n/a	chr7:5893027-5893038
9	CEBPB	chr7:5890537-5890656	IMR90	lung:	n/a	chr7:5890571-5890582
10	CEBPB	chr7:5892975-5893180	HepG2	liver:	n/a	chr7:5893027-5893038
11	CEBPB	chr7:5893018-5893091	Hela-S3	cervix:	n/a	chr7:5893027-5893038
12	CEBPB	chr7:5929893-5930182	K562	blood:	n/a	n/a
13	CEBPB	chr7:5929312-5929450	IMR90	lung:	n/a	n/a
14	CEBPB	chr7:5891809-5891870	IMR90	lung:	n/a	n/a
15	CEBPB	chr7:5892977-5893179	IMR90	lung:	n/a	chr7:5893027-5893038
16	CEBPB	chr7:5890537-5890700	A549	lung:	n/a	chr7:5890571-5890582
17	CEBPB	chr7:5890535-5890604	H1-hESC	embryonic stem cell:	n/a	chr7:5890571-5890582
18	CEBPB	chr7:5892975-5893174	A549	lung:	n/a	chr7:5893027-5893038
19	CEBPB	chr7:5912087-5912368	IMR90	lung:	n/a	n/a
20	CEBPB	chr7:5890492-5890732	K562	blood:	n/a	chr7:5890571-5890582
21	CEBPB	chr7:5896180-5896389	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr7:5890460-5890688	HepG2	liver:	n/a	chr7:5890571-5890582
23	CEBPB	chr7:5892913-5893127	H1-hESC	embryonic stem cell:	n/a	chr7:5893027-5893038
24	CHD2	chr7:5894459-5894465	HepG2	liver:	n/a	n/a
25	CTCF	chr7:5896135-5896379	GM10248	blood:	n/a	n/a
26	CTCF	chr7:5905000-5905150	A549	lung:	n/a	n/a
27	CTCF	chr7:5896200-5896350	HCPEpiC	choroid plexus:	n/a	n/a
28	CTCF	chr7:5908800-5908950	HCPEpiC	choroid plexus:	n/a	chr7:5908846-5908864 chr7:5908849-5908862
29	CTCF	chr7:5896180-5896330	AG04450	lung:	n/a	n/a
30	CTCF	chr7:5918870-5918898	GM13976	blood:	n/a	n/a
31	CTCF	chr7:5904030-5904145	MCF-7	breast:	n/a	n/a
32	CTCF	chr7:5908760-5908910	HEK293	kidney:	n/a	chr7:5908846-5908864 chr7:5908849-5908862
33	CTCF	chr7:5896114-5896386	Hela-S3	cervix:	n/a	n/a
34	CTCF	chr7:5905027-5905179	K562	blood:	n/a	n/a
35	CTCF	chr7:5880420-5880570	MCF-7	breast:	n/a	chr7:5880500-5880513 chr7:5880497-5880515
36	CTCF	chr7:5896240-5896390	NHDF-neo	bronchial:	n/a	n/a
37	CTCF	chr7:5895860-5896010	AG09319	gingival:	n/a	n/a
38	CTCF	chr7:5896140-5896290	GM06990	blood:	n/a	n/a
39	CTCF	chr7:5896160-5896310	HepG2	liver:	n/a	n/a
40	CTCF	chr7:5896093-5896386	Pancreas_OC	pancreas:	n/a	n/a
41	CTCF	chr7:5896200-5896350	GM12874	blood:	n/a	n/a
42	CTCF	chr7:5896094-5896415	HepG2	liver:	n/a	n/a
43	CTCF	chr7:5896180-5896330	HVMF	connective:	n/a	n/a
44	CTCF	chr7:5896220-5896370	GM12867	blood:	n/a	n/a
45	CTCF	chr7:5896075-5896460	A549	lung:	n/a	n/a
46	CTCF	chr7:5896001-5896381	A549	lung:	n/a	n/a
47	CTCF	chr7:5896200-5896350	K562	blood:	n/a	n/a
48	CTCF	chr7:5905030-5905122	GM13977	blood:	n/a	n/a
49	CTCF	chr7:5880442-5880562	H1-hESC	embryonic stem cell:	n/a	chr7:5880500-5880513 chr7:5880497-5880515
50	CTCF	chr7:5896099-5896398	Medullo	brain:	n/a	n/a

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:5919583-5919633	HRE	kidney:	n/a
2	chr7:5919583-5919633	HRE	kidney:	n/a
3	chr7:5887023-5887073	SK-N-MC	brain:	n/a
4	chr7:5911701-5911751	ECC-1	luminal epithelium:	n/a
5	chr7:5911800-5911850	HNPCEpiC	eye:	n/a
6	chr7:5919012-5919062	Hepatocyte	liver:	n/a
7	chr7:5920635-5920685	ProgFib	skin:	n/a
8	chr7:5888077-5888127	HCF	heart:	n/a
9	chr7:5890037-5890087	Hepatocyte	liver:	n/a
10	chr7:5919012-5919062	AG10803	skin:	n/a
11	chr7:5919012-5919062	HRPEpiC	eye:	n/a
12	chr7:5887023-5887073	BE2_C	brain:	n/a
13	chr7:5919589-5919639	AG04450	lung:	fetal
14	chr7:5885244-5885294	NT2-D1	testis:	n/a
15	chr7:5920635-5920685	GM12891	blood:	n/a
16	chr7:5911900-5911950	HNPCEpiC	eye:	n/a
17	chr7:5883645-5883695	IMR90	lung:	fetal
18	chr7:5890037-5890087	HEK293	kidney:	embryo
19	chr7:5919589-5919639	BE2_C	brain:	n/a
20	chr7:5886722-5886772	HAEpiC	amniotic membrane:	n/a
21	chr7:5890037-5890087	MCF-7	breast:	n/a
22	chr7:5919583-5919633	T-47D	breast:	n/a
23	chr7:5886722-5886772	PrEC	prostate:	n/a
24	chr7:5883645-5883695	HL-60	blood:	n/a
25	chr7:5911900-5911950	NHBE	bronchial:	n/a
26	chr7:5911800-5911850	Hela-S3	cervix:	n/a
27	chr7:5919012-5919062	SK-N-SH	brain:	n/a
28	chr7:5919583-5919633	GM19239	blood:	n/a
29	chr7:5920635-5920685	HRCEpiC	kidney:	n/a
30	chr7:5919583-5919633	HepG2	liver:	n/a
31	chr7:5888077-5888127	NB4	blood:	n/a
32	chr7:5919583-5919633	PFSK-1	brain:	n/a
33	chr7:5919589-5919639	NH-A	brain:	n/a
34	chr7:5919589-5919639	HCF	heart:	n/a
35	chr7:5890037-5890087	H1-hESC	embryonic stem cell:	embryo
36	chr7:5919012-5919062	HPAEpiC	pulmonary alveolar:	n/a
37	chr7:5883645-5883695	ovcar-3	ovarian:	n/a
38	chr7:5911900-5911950	A549	lung:	n/a
39	chr7:5887023-5887073	GM12878	blood:	n/a
40	chr7:5890037-5890087	HMEC	breast:	n/a
41	chr7:5919583-5919633	NT2-D1	testis:	n/a
42	chr7:5919589-5919639	ovcar-3	ovarian:	n/a
43	chr7:5911800-5911850	HEEpiC	esophagus:	n/a
44	chr7:5890037-5890087	HPAEpiC	pulmonary alveolar:	n/a
45	chr7:5887023-5887073	Jurkat	blood:	n/a
46	chr7:5919012-5919062	HNPCEpiC	eye:	n/a
47	chr7:5919012-5919062	NB4	blood:	n/a
48	chr7:5911701-5911751	ProgFib	skin:	n/a
49	chr7:5911800-5911850	BJ	skin:	n/a
50	chr7:5885244-5885294	GM12891	blood:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:5877107..5878733-chr7:5880762..5883645,2	K562	blood:
2	chr7:5877107..5878733-chr7:5880762..5883645,2	K562	blood:
3	chr7:5875724..5878623-chr7:5880700..5882793,2	MCF-7	breast:
4	chr7:5921888..5923776-chr7:6615172..6617060,2	K562	blood:
5	chr7:5877192..5879014-chr7:6172405..6175361,2	K562	blood:
6	chr7:5875724..5878623-chr7:5880700..5882793,2	MCF-7	breast:
7	chr7:5895754..5896691-chr7:6036473..6037181,2	MCF-7	breast:
8	chr7:5896217..5898583-chr7:97641356..97642858,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OCM-3	chr7:5878701-5878783	NONHSAT118942
2	lnc-OCM-3	chr7:5893738-5893857	NONHSAT118944
3	lnc-OCM-3	chr7:5879580-5879706	NONHSAT118944
4	lnc-OCM-3	chr7:5878820-5878850	NONHSAT118948
5	lnc-OCM-3	chr7:5880321-5880487	NONHSAT118944
6	lnc-RSPH10B-1	chr7:5911384-5911681	NONHSAT118956

No data

Variant related genes	Relation type
OCM	TF binding region
ZNF815P	TF binding region
RN7SL556P	TF binding region
OCM	CpG island
ZNF815P	CpG island
RN7SL556P	CpG island

Extended variants
information (count: 3573 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:3573 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs186637499	chr7:5874854-5874855	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs111825367	chr7:5874867-5874868	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs199737789	chr7:5874904-5874905	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs4521662	chr7:5874907-5874908	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs572988980	chr7:5874908-5874909	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs540275996	chr7:5874914-5874915	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs564936645	chr7:5874932-5874933	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs576783488	chr7:5874946-5874947	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs560402345	chr7:5874983-5874984	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs544913919	chr7:5874988-5874989	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs570299219	chr7:5875004-5875005	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs563020330	chr7:5875049-5875050	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs143895647	chr7:5875053-5875054	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs146596705	chr7:5875070-5875071	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs561085076	chr7:5875081-5875082	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs7790960	chr7:5875097-5875098	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs546679073	chr7:5875104-5875105	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs571280454	chr7:5875110-5875111	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs7792068	chr7:5875111-5875112	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs550878826	chr7:5875120-5875121	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs117811884	chr7:5875136-5875137	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs541065192	chr7:5875142-5875143	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs536487441	chr7:5875150-5875151	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs377641941	chr7:5875177-5875178	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs369217185	chr7:5875214-5875215	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs58422033	chr7:5875235-5875236	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs148489460	chr7:5875238-5875239	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs555167726	chr7:5875241-5875242	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs534035011	chr7:5875249-5875250	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs75198726	chr7:5875252-5875253	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs145929806	chr7:5875259-5875260	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs551706135	chr7:5875268-5875269	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs544266888	chr7:5875274-5875275	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs544776987	chr7:5875275-5875276	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs139825678	chr7:5875290-5875291	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs542463515	chr7:5875344-5875345	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs560678130	chr7:5875354-5875355	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs10226026	chr7:5875372-5875373	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs10256237	chr7:5875373-5875374	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs564950417	chr7:5875374-5875375	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs190369908	chr7:5875392-5875393	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs542556543	chr7:5875395-5875396	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs550296052	chr7:5875402-5875403	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs569176477	chr7:5875404-5875405	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs529945499	chr7:5875408-5875409	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs561278090	chr7:5875418-5875419	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs566343297	chr7:5875423-5875424	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs192859449	chr7:5875456-5875457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs558663240	chr7:5875458-5875459	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs376517543	chr7:5875472-5875473	Weak transcription Enhancers	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:334 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:5863600-5896800	Weak transcription	Esophagus	oesophagus
2	chr7:5863800-5879200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr7:5863800-5881600	Weak transcription	Fetal Intestine Small	intestine
4	chr7:5863800-5887000	Weak transcription	Primary B cells from cord blood	blood
5	chr7:5863800-5891400	Weak transcription	Liver	Liver
6	chr7:5863800-5891400	Weak transcription	Brain Hippocampus Middle	brain
7	chr7:5863800-5896200	Weak transcription	Adipose Nuclei	Adipose
8	chr7:5864000-5880400	Weak transcription	Brain Substantia Nigra	brain
9	chr7:5864200-5880400	Weak transcription	Primary B cells from peripheral blood	blood
10	chr7:5864200-5893600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr7:5867600-5885000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
12	chr7:5869200-5881600	Weak transcription	Fetal Stomach	stomach
13	chr7:5871200-5882600	Weak transcription	Fetal Brain Male	brain
14	chr7:5871400-5878600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr7:5871400-5878600	Weak transcription	Monocytes-CD14+_RO01746	blood
16	chr7:5871400-5878800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr7:5871400-5881200	Weak transcription	Primary monocytes fromperipheralblood	blood
18	chr7:5871400-5890600	Weak transcription	Brain Germinal Matrix	brain
19	chr7:5871400-5904600	Weak transcription	Spleen	Spleen
20	chr7:5871600-5889200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr7:5871600-5891800	Weak transcription	Cortex derived primary cultured neurospheres	brain
22	chr7:5871600-5896400	Weak transcription	Fetal Brain Female	brain
23	chr7:5872000-5877400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
24	chr7:5872200-5877400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
25	chr7:5872200-5877400	Enhancers	Primary T killer memory cells from peripheral blood	blood
26	chr7:5872600-5877200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
27	chr7:5872600-5877400	Enhancers	Primary T helper naive cells from peripheral blood	blood
28	chr7:5872600-5877400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
29	chr7:5872800-5876400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
30	chr7:5873200-5875600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
31	chr7:5873200-5896200	Weak transcription	Lung	lung
32	chr7:5873400-5878800	Weak transcription	Primary neutrophils fromperipheralblood	blood
33	chr7:5873800-5878800	Enhancers	Primary T helper cells fromperipheralblood	blood
34	chr7:5873800-5881600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
35	chr7:5874200-5875600	Enhancers	Primary T helper cells PMA-I stimulated	--
36	chr7:5874200-5875800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
37	chr7:5874400-5877400	Enhancers	Primary T cells from cord blood	blood
38	chr7:5874400-5878400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr7:5874400-5881600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr7:5874600-5878400	Weak transcription	Primary hematopoietic stem cells	blood
41	chr7:5874800-5875200	Genic enhancers	Primary T cells fromperipheralblood	blood
42	chr7:5875200-5878200	Enhancers	Primary T cells fromperipheralblood	blood
43	chr7:5875400-5896600	Weak transcription	Brain Inferior Temporal Lobe	brain
44	chr7:5875600-5876000	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
45	chr7:5875600-5876000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
46	chr7:5875800-5876000	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
47	chr7:5876000-5876200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
48	chr7:5876000-5878000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
49	chr7:5876000-5878400	Enhancers	Primary T helper cells PMA-I stimulated	--
50	chr7:5876200-5876400	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood

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