Variant report

Variant	esv274969
Chromosome Location	chr7:5936888-5965441
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr7:5938735-5938983	GM12878	blood:	n/a	n/a
2	BATF	chr7:5938176-5938390	GM12878	blood:	n/a	n/a
3	BCL11A	chr7:5938179-5938410	GM12878	blood:	n/a	n/a
4	BCL11A	chr7:5938072-5938321	GM12878	blood:	n/a	n/a
5	BHLHE40	chr7:5938233-5938412	K562	blood:	n/a	n/a
6	BRCA1	chr7:5938138-5938423	Hela-S3	cervix:	n/a	n/a
7	CBX3	chr7:5938925-5939374	K562	blood:	n/a	n/a
8	CBX3	chr7:5937356-5938688	K562	blood:	n/a	n/a
9	CBX3	chr7:5938092-5938432	K562	blood:	n/a	n/a
10	CEBPB	chr7:5942532-5942815	K562	blood:	n/a	chr7:5942734-5942743 chr7:5942734-5942745
11	CHD2	chr7:5938146-5938417	Hela-S3	cervix:	n/a	n/a
12	CREB1	chr7:5938058-5938399	A549	lung:	n/a	n/a
13	CREB1	chr7:5938052-5938355	HepG2	liver:	n/a	n/a
14	CTCF	chr7:5938120-5938270	HRPEpiC	eye:	n/a	n/a
15	CTCF	chr7:5938762-5938903	GM13976	blood:	n/a	n/a
16	CTCF	chr7:5938158-5938388	MCF-7	breast:	n/a	chr7:5938264-5938273
17	CTCF	chr7:5938120-5938270	HepG2	liver:	n/a	n/a
18	CTCF	chr7:5938120-5938270	HMEC	breast:	n/a	n/a
19	CTCF	chr7:5938120-5938270	HA-sp	spinal cord:	n/a	n/a
20	CTCF	chr7:5938160-5938310	HUVEC	blood vessel:	n/a	chr7:5938264-5938273
21	CTCF	chr7:5938154-5938340	HepG2	liver:	n/a	chr7:5938264-5938273
22	CTCF	chr7:5937986-5938565	K562	blood:	n/a	chr7:5938264-5938273
23	CTCF	chr7:5938234-5938322	LNCaP	prostate:	n/a	chr7:5938264-5938273
24	CTCF	chr7:5938200-5938350	HAc	cerebellar:	n/a	chr7:5938264-5938273
25	CTCF	chr7:5938180-5938330	HPAF	blood vessel:	n/a	chr7:5938264-5938273
26	CTCF	chr7:5938216-5938380	HUVEC	blood vessel:	n/a	chr7:5938264-5938273
27	CTCF	chr7:5938180-5938330	GM06990	blood:	n/a	chr7:5938264-5938273
28	CTCF	chr7:5938160-5938310	GM12868	blood:	n/a	chr7:5938264-5938273
29	CTCF	chr7:5938120-5938270	HUVEC	blood vessel:	n/a	n/a
30	CTCF	chr7:5959212-5959240	GM13976	blood:	n/a	n/a
31	CTCF	chr7:5938163-5938395	MCF-7	breast:	n/a	chr7:5938264-5938273
32	CTCF	chr7:5938186-5938337	HepG2	liver:	n/a	chr7:5938264-5938273
33	CTCF	chr7:5938160-5938310	AG04450	lung:	n/a	chr7:5938264-5938273
34	CTCF	chr7:5938146-5938449	K562	blood:	n/a	chr7:5938264-5938273
35	CTCF	chr7:5938180-5938330	Caco-2	colon:	n/a	chr7:5938264-5938273
36	CTCF	chr7:5938208-5938359	Pancreas_OC	pancreas:	n/a	chr7:5938264-5938273
37	CTCF	chr7:5938120-5938270	AG04449	skin:	n/a	n/a
38	CTCF	chr7:5938120-5938270	HEEpiC	esophagus:	n/a	n/a
39	CTCF	chr7:5938101-5938490	K562	blood:	n/a	chr7:5938264-5938273
40	CTCF	chr7:5938201-5938353	SK-N-SH_RA	brain:	n/a	chr7:5938264-5938273
41	CTCF	chr7:5965247-5965339	GM20000	blood:	n/a	n/a
42	CTCF	chr7:5938180-5938330	HBMEC	blood vessel:	n/a	chr7:5938264-5938273
43	CTCF	chr7:5938120-5938270	HMF	breast:	n/a	n/a
44	CTCF	chr7:5938180-5938330	NHLF	lung:	n/a	chr7:5938264-5938273
45	CTCF	chr7:5938220-5938370	WI-38	lung:	n/a	chr7:5938264-5938273
46	CTCF	chr7:5938120-5938270	Caco-2	colon:	n/a	n/a
47	CTCF	chr7:5938200-5938350	HVMF	connective:	n/a	chr7:5938264-5938273
48	CTCF	chr7:5938160-5938360	T-47D	breast:	n/a	chr7:5938264-5938273
49	CTCF	chr7:5938140-5938290	GM12867	blood:	n/a	chr7:5938264-5938273
50	CTCF	chr7:5939258-5939380	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:5938288-5938338	HRE	kidney:	n/a
2	chr7:5938288-5938338	HRE	kidney:	n/a
3	chr7:5938204-5938254	MCF10A-Er-Src	breast:	n/a
4	chr7:5938227-5938277	GM12892	blood:	n/a
5	chr7:5938293-5938343	AG04450	lung:	fetal
6	chr7:5938288-5938338	PrEC	prostate:	n/a
7	chr7:5941157-5941207	ProgFib	skin:	n/a
8	chr7:5938288-5938338	HUVEC	blood vessel:	n/a
9	chr7:5938193-5938243	HUVEC	blood vessel:	n/a
10	chr7:5937190-5937240	HIPEpiC	eye:	n/a
11	chr7:5939791-5939841	CMK	blood:	n/a
12	chr7:5937190-5937240	SKMC	muscle:	n/a
13	chr7:5938293-5938343	HRCEpiC	kidney:	n/a
14	chr7:5939791-5939841	AG04449	skin:	fetal
15	chr7:5963438-5963488	HAEpiC	amniotic membrane:	n/a
16	chr7:5937433-5937483	HUVEC	blood vessel:	n/a
17	chr7:5937190-5937240	HAEpiC	amniotic membrane:	n/a
18	chr7:5938204-5938254	ECC-1	luminal epithelium:	n/a
19	chr7:5938193-5938243	HAEpiC	amniotic membrane:	n/a
20	chr7:5939791-5939841	NHBE	bronchial:	n/a
21	chr7:5963438-5963488	PFSK-1	brain:	n/a
22	chr7:5938204-5938254	NH-A	brain:	n/a
23	chr7:5938204-5938254	ovcar-3	ovarian:	n/a
24	chr7:5938195-5938245	HNPCEpiC	eye:	n/a
25	chr7:5938288-5938338	HIPEpiC	eye:	n/a
26	chr7:5963438-5963488	Jurkat	blood:	n/a
27	chr7:5938195-5938245	CMK	blood:	n/a
28	chr7:5938293-5938343	HPAEpiC	pulmonary alveolar:	n/a
29	chr7:5938293-5938343	RPTEC	kidney:	n/a
30	chr7:5963438-5963488	NHBE	bronchial:	n/a
31	chr7:5937486-5937536	Caco-2	colon:	n/a
32	chr7:5938293-5938343	GM12878	blood:	n/a
33	chr7:5963438-5963488	ProgFib	skin:	n/a
34	chr7:5938204-5938254	NHDF-neo	bronchial:	n/a
35	chr7:5963438-5963488	RPTEC	kidney:	n/a
36	chr7:5937190-5937240	HRPEpiC	eye:	n/a
37	chr7:5938227-5938277	BE2_C	brain:	n/a
38	chr7:5938195-5938245	Jurkat	blood:	n/a
39	chr7:5937190-5937240	Hela-S3	cervix:	n/a
40	chr7:5941157-5941207	HCF	heart:	n/a
41	chr7:5941157-5941207	HEK293	kidney:	embryo
42	chr7:5938193-5938243	RPTEC	kidney:	n/a
43	chr7:5938293-5938343	Jurkat	blood:	n/a
44	chr7:5938195-5938245	MCF-7	breast:	n/a
45	chr7:5938293-5938343	Hepatocyte	liver:	n/a
46	chr7:5938195-5938245	AG09309	skin:	n/a
47	chr7:5963438-5963488	HNPCEpiC	eye:	n/a
48	chr7:5938193-5938243	NHBE	bronchial:	n/a
49	chr7:5938193-5938243	SK-N-SH	brain:	n/a
50	chr7:5963438-5963488	U87	brain:	n/a

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OCM-2	chr7:5964372-5964445	NONHSAT118958
2	lnc-OCM-2	chr7:5965263-5965571	NONHSAT118958

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

Extended variants
information (count: 1289 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:1289 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs60313149	chr7:5936904-5936905	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs182478745	chr7:5936905-5936906	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs58793660	chr7:5936956-5936957	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs113626345	chr7:5936968-5936969	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs536574532	chr7:5937019-5937020	Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs548664307	chr7:5937022-5937023	Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs567247572	chr7:5937030-5937031	Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs144052610	chr7:5937069-5937070	Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs555001592	chr7:5937137-5937138	Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs553083573	chr7:5937148-5937149	Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs571402512	chr7:5937179-5937180	Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs533563560	chr7:5937192-5937193	Active TSS Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
13	rs57888661	chr7:5937240-5937241	Active TSS Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
14	rs377691349	chr7:5937244-5937245	Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs58687839	chr7:5937245-5937246	Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs28525991	chr7:5937285-5937286	Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs28417143	chr7:5937298-5937299	Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs28580246	chr7:5937301-5937302	Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs115443965	chr7:5937373-5937374	Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs543315875	chr7:5937378-5937379	Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs185857009	chr7:5937383-5937384	Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs113328154	chr7:5937384-5937385	Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs555003999	chr7:5937392-5937393	Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs188823627	chr7:5937398-5937399	Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs540258254	chr7:5937401-5937402	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs386709787	chr7:5937403-5937404	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs201432244	chr7:5937404-5937405	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs28437675	chr7:5937412-5937413	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs28558301	chr7:5937428-5937429	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs193209952	chr7:5937444-5937445	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
31	rs549259903	chr7:5937458-5937459	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
32	rs567479304	chr7:5937485-5937486	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs111717448	chr7:5937508-5937509	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
34	rs528078767	chr7:5937535-5937536	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
35	rs546636011	chr7:5937585-5937586	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs185221717	chr7:5937597-5937598	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs189001055	chr7:5937609-5937610	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs538742917	chr7:5937658-5937659	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs557233162	chr7:5937679-5937680	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs569424580	chr7:5937722-5937723	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs536493014	chr7:5937743-5937744	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs555221726	chr7:5937802-5937803	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs573233337	chr7:5937819-5937820	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs540198203	chr7:5937821-5937822	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs147761489	chr7:5937864-5937865	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs576876153	chr7:5937892-5937893	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs529998787	chr7:5937902-5937903	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs149857071	chr7:5937949-5937950	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs530712240	chr7:5937963-5937964	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs370090761	chr7:5938067-5938068	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:78)

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
Acute myeloid leukemia	21251322	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:678 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:5895400-5938000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr7:5899200-5937400	Weak transcription	Primary T helper cells fromperipheralblood	blood
3	chr7:5933600-5937800	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr7:5935200-5937400	Weak transcription	HepG2	liver
5	chr7:5935200-5937800	Weak transcription	A549	lung
6	chr7:5935200-5951600	Weak transcription	HMEC	breast
7	chr7:5936800-5937000	Enhancers	Sigmoid Colon	Sigmoid Colon
8	chr7:5936800-5937000	Enhancers	GM12878-XiMat	blood
9	chr7:5936800-5937200	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr7:5936800-5937200	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr7:5937000-5937400	Enhancers	Brain Inferior Temporal Lobe	brain
12	chr7:5937000-5938200	Active TSS	HUES6 Cell Line	embryonic stem cell
13	chr7:5937000-5938200	Active TSS	GM12878-XiMat	blood
14	chr7:5937200-5937400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr7:5937200-5937400	Enhancers	Dnd41	blood
16	chr7:5937200-5938200	Active TSS	ES-I3 Cell Line	embryonic stem cell
17	chr7:5937400-5937600	Active TSS	iPS-18 Cell Line	embryonic stem cell
18	chr7:5937400-5937600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr7:5937400-5937600	Enhancers	Fetal Heart	heart
20	chr7:5937400-5937600	Flanking Active TSS	HepG2	liver
21	chr7:5937400-5937800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr7:5937400-5937800	Enhancers	Primary B cells from peripheral blood	blood
23	chr7:5937400-5937800	Enhancers	Primary T cells fromperipheralblood	blood
24	chr7:5937400-5937800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
25	chr7:5937400-5937800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
26	chr7:5937400-5938000	Enhancers	Primary T helper cells fromperipheralblood	blood
27	chr7:5937400-5938000	Flanking Active TSS	Dnd41	blood
28	chr7:5937400-5938200	Active TSS	iPS-15b Cell Line	embryonic stem cell
29	chr7:5937400-5938200	Active TSS	Brain Anterior Caudate	brain
30	chr7:5937400-5938200	Active TSS	Brain Cingulate Gyrus	brain
31	chr7:5937400-5938200	Enhancers	Brain Substantia Nigra	brain
32	chr7:5937400-5938400	Active TSS	HUES48 Cell Line	embryonic stem cell
33	chr7:5937400-5938400	Active TSS	iPS-20b Cell Line	embryonic stem cell
34	chr7:5937400-5938400	Active TSS	Adipose Nuclei	Adipose
35	chr7:5937400-5938400	Active TSS	Brain Hippocampus Middle	brain
36	chr7:5937400-5938400	Active TSS	Brain Inferior Temporal Lobe	brain
37	chr7:5937400-5938400	Active TSS	Duodenum Mucosa	Duodenum
38	chr7:5937400-5938400	Active TSS	Skeletal Muscle Male	skeletal muscle
39	chr7:5937400-5938400	Active TSS	Skeletal Muscle Female	skeletal muscle
40	chr7:5937400-5938400	Active TSS	Hela-S3	cervix
41	chr7:5937400-5938400	Active TSS	Monocytes-CD14+_RO01746	blood
42	chr7:5937400-5939600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr7:5937600-5937800	Enhancers	Primary monocytes fromperipheralblood	blood
44	chr7:5937600-5937800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
45	chr7:5937600-5937800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr7:5937600-5937800	Enhancers	Fetal Muscle Trunk	muscle
47	chr7:5937600-5937800	Enhancers	Fetal Muscle Leg	muscle
48	chr7:5937600-5937800	Enhancers	Spleen	Spleen
49	chr7:5937600-5938000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
50	chr7:5937600-5938000	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin

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