Variant report

Variant	nsv1026461
Chromosome Location	chr7:5891977-5970922
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1022)
CpG islands
(count:1284)
Chromatin interactive
region (count:3)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1022 , 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	chr7:5896136-5896348	GM12878	blood:	n/a	n/a
3	BATF	chr7:5938176-5938390	GM12878	blood:	n/a	n/a
4	BATF	chr7:5938735-5938983	GM12878	blood:	n/a	n/a
5	BCL11A	chr7:5938072-5938321	GM12878	blood:	n/a	n/a
6	BCL11A	chr7:5938179-5938410	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	BRCA1	chr7:5896176-5896337	Hela-S3	cervix:	n/a	n/a
11	BRCA1	chr7:5938138-5938423	Hela-S3	cervix:	n/a	n/a
12	CBX3	chr7:5938092-5938432	K562	blood:	n/a	n/a
13	CBX3	chr7:5937356-5938688	K562	blood:	n/a	n/a
14	CBX3	chr7:5938925-5939374	K562	blood:	n/a	n/a
15	CEBPB	chr7:5892977-5893179	IMR90	lung:	n/a	chr7:5893027-5893038
16	CEBPB	chr7:5893018-5893091	Hela-S3	cervix:	n/a	chr7:5893027-5893038
17	CEBPB	chr7:5929893-5930182	K562	blood:	n/a	n/a
18	CEBPB	chr7:5892975-5893174	A549	lung:	n/a	chr7:5893027-5893038
19	CEBPB	chr7:5892913-5893127	H1-hESC	embryonic stem cell:	n/a	chr7:5893027-5893038
20	CEBPB	chr7:5912087-5912368	IMR90	lung:	n/a	n/a
21	CEBPB	chr7:5892955-5893172	K562	blood:	n/a	chr7:5893027-5893038
22	CEBPB	chr7:5942532-5942815	K562	blood:	n/a	chr7:5942734-5942743 chr7:5942734-5942745
23	CEBPB	chr7:5892975-5893180	HepG2	liver:	n/a	chr7:5893027-5893038
24	CEBPB	chr7:5896180-5896389	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr7:5929312-5929450	IMR90	lung:	n/a	n/a
26	CHD2	chr7:5894459-5894465	HepG2	liver:	n/a	n/a
27	CHD2	chr7:5938146-5938417	Hela-S3	cervix:	n/a	n/a
28	CREB1	chr7:5938052-5938355	HepG2	liver:	n/a	n/a
29	CREB1	chr7:5938058-5938399	A549	lung:	n/a	n/a
30	CTCF	chr7:5896160-5896310	AG04449	skin:	n/a	n/a
31	CTCF	chr7:5904030-5904145	MCF-7	breast:	n/a	n/a
32	CTCF	chr7:5896160-5896310	GM12865	blood:	n/a	n/a
33	CTCF	chr7:5938140-5938290	HFF	foreskin:	n/a	chr7:5938264-5938273
34	CTCF	chr7:5938160-5938310	GM12869	blood:	n/a	chr7:5938264-5938273
35	CTCF	chr7:5938158-5938388	MCF-7	breast:	n/a	chr7:5938264-5938273
36	CTCF	chr7:5895829-5896605	A549	lung:	n/a	n/a
37	CTCF	chr7:5938120-5938270	HMEC	breast:	n/a	n/a
38	CTCF	chr7:5896200-5896350	HBMEC	blood vessel:	n/a	n/a
39	CTCF	chr7:5938160-5938310	HEK293	kidney:	n/a	chr7:5938264-5938273
40	CTCF	chr7:5938160-5938310	GM12868	blood:	n/a	chr7:5938264-5938273
41	CTCF	chr7:5896099-5896398	Medullo	brain:	n/a	n/a
42	CTCF	chr7:5896175-5896404	GM19238	blood:	n/a	n/a
43	CTCF	chr7:5938100-5938250	HFF-Myc	foreskin:	n/a	n/a
44	CTCF	chr7:5896147-5896389	A549	lung:	n/a	n/a
45	CTCF	chr7:5938160-5938310	GM12866	blood:	n/a	chr7:5938264-5938273
46	CTCF	chr7:5938160-5938310	HBMEC	blood vessel:	n/a	chr7:5938264-5938273
47	CTCF	chr7:5904951-5905249	K562	blood:	n/a	n/a
48	CTCF	chr7:5938180-5938330	GM12874	blood:	n/a	chr7:5938264-5938273
49	CTCF	chr7:5938160-5938310	GM12864	blood:	n/a	chr7:5938264-5938273
50	CTCF	chr7:5896280-5896430	NHDF-neo	bronchial:	n/a	n/a

(count:1284 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:5919012-5919062	ECC-1	luminal epithelium:	n/a
2	chr7:5920535-5920585	NHDF-neo	bronchial:	n/a
3	chr7:5911701-5911751	NHBE	bronchial:	n/a
4	chr7:5919012-5919062	ECC-1	luminal epithelium:	n/a
5	chr7:5920535-5920585	NHDF-neo	bronchial:	n/a
6	chr7:5911701-5911751	NHBE	bronchial:	n/a
7	chr7:5919012-5919062	H1-hESC	embryonic stem cell:	embryo
8	chr7:5919589-5919639	HL-60	blood:	n/a
9	chr7:5938195-5938245	ECC-1	luminal epithelium:	n/a
10	chr7:5919012-5919062	Jurkat	blood:	n/a
11	chr7:5939791-5939841	Jurkat	blood:	n/a
12	chr7:5919589-5919639	ovcar-3	ovarian:	n/a
13	chr7:5920635-5920685	ECC-1	luminal epithelium:	n/a
14	chr7:5937433-5937483	SK-N-SH_RA	brain:	n/a
15	chr7:5938227-5938277	SK-N-SH_RA	brain:	n/a
16	chr7:5920635-5920685	GM12878	blood:	n/a
17	chr7:5938288-5938338	HNPCEpiC	eye:	n/a
18	chr7:5938193-5938243	HRPEpiC	eye:	n/a
19	chr7:5938227-5938277	LNCaP	prostate:	n/a
20	chr7:5941157-5941207	MCF-7	breast:	n/a
21	chr7:5938195-5938245	H1-hESC	embryonic stem cell:	embryo
22	chr7:5937433-5937483	K562	blood:	n/a
23	chr7:5938195-5938245	Hepatocyte	liver:	n/a
24	chr7:5941157-5941207	PANC-1	pancreas:	n/a
25	chr7:5938293-5938343	SK-N-SH_RA	brain:	n/a
26	chr7:5911701-5911751	NB4	blood:	n/a
27	chr7:5937433-5937483	HL-60	blood:	n/a
28	chr7:5963438-5963488	AG04450	lung:	fetal
29	chr7:5941157-5941207	HNPCEpiC	eye:	n/a
30	chr7:5935002-5935052	T-47D	breast:	n/a
31	chr7:5919589-5919639	HCF	heart:	n/a
32	chr7:5941157-5941207	HIPEpiC	eye:	n/a
33	chr7:5938204-5938254	HCPEpiC	choroid plexus:	n/a
34	chr7:5919012-5919062	MCF10A-Er-Src	breast:	n/a
35	chr7:5919583-5919633	NH-A	brain:	n/a
36	chr7:5938204-5938254	Hepatocyte	liver:	n/a
37	chr7:5941157-5941207	SAEC	small airway:	n/a
38	chr7:5911701-5911751	HEEpiC	esophagus:	n/a
39	chr7:5938293-5938343	HMEC	breast:	n/a
40	chr7:5937486-5937536	MCF-7	breast:	n/a
41	chr7:5935002-5935052	HRPEpiC	eye:	n/a
42	chr7:5937190-5937240	NT2-D1	testis:	n/a
43	chr7:5920535-5920585	IMR90	lung:	fetal
44	chr7:5938204-5938254	A549	lung:	n/a
45	chr7:5920535-5920585	ProgFib	skin:	n/a
46	chr7:5937190-5937240	HUVEC	blood vessel:	n/a
47	chr7:5941157-5941207	BJ	skin:	n/a
48	chr7:5911900-5911950	Hepatocyte	liver:	n/a
49	chr7:5963438-5963488	ovcar-3	ovarian:	n/a
50	chr7:5938195-5938245	NHBE	bronchial:	n/a

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

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

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

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

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: 4112 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:4112 , 50 per page) page: 1 2 3 4 5 6 7 ... 83

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs143245402	chr7:5891980-5891981	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs555046819	chr7:5891995-5891996	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs73052599	chr7:5892016-5892017	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs527887885	chr7:5892027-5892028	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs552693638	chr7:5892034-5892035	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs571265747	chr7:5892058-5892059	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs137879003	chr7:5892059-5892060	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs554821461	chr7:5892081-5892082	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs556708404	chr7:5892088-5892089	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs111523725	chr7:5892106-5892107	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs6944585	chr7:5892125-5892126	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs117856560	chr7:5892134-5892135	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
13	rs572753021	chr7:5892135-5892136	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs10258041	chr7:5892142-5892143	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs139434990	chr7:5892152-5892153	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs201512593	chr7:5892153-5892154	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs558686299	chr7:5892160-5892161	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs117027786	chr7:5892174-5892175	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs539843287	chr7:5892186-5892187	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs6463520	chr7:5892190-5892191	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs562904455	chr7:5892197-5892198	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs530110513	chr7:5892198-5892199	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs10243003	chr7:5892200-5892201	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs560772512	chr7:5892202-5892203	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs112221535	chr7:5892224-5892225	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs552517069	chr7:5892230-5892231	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs571001384	chr7:5892236-5892237	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs112856072	chr7:5892261-5892262	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs540033693	chr7:5892271-5892272	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs532139556	chr7:5892274-5892275	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs550637863	chr7:5892300-5892301	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs186296751	chr7:5892301-5892302	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs6463521	chr7:5892303-5892304	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs554102403	chr7:5892339-5892340	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs150660473	chr7:5892340-5892341	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs538024370	chr7:5892365-5892366	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs534067161	chr7:5892396-5892397	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs139887929	chr7:5892406-5892407	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs576953254	chr7:5892419-5892420	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs189573009	chr7:5892425-5892426	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs556695462	chr7:5892442-5892443	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs574942734	chr7:5892451-5892452	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs542256120	chr7:5892453-5892454	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs560482280	chr7:5892463-5892464	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs544144725	chr7:5892592-5892593	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs377330538	chr7:5892605-5892606	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs147967064	chr7:5892611-5892612	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
48	rs564562941	chr7:5892615-5892616	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs113129018	chr7:5892620-5892621	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs13228584	chr7:5892690-5892691	Weak transcription 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:883 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:5863600-5896800	Weak transcription	Esophagus	oesophagus
2	chr7:5863800-5896200	Weak transcription	Adipose Nuclei	Adipose
3	chr7:5864200-5893600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr7:5871400-5904600	Weak transcription	Spleen	Spleen
5	chr7:5871600-5896400	Weak transcription	Fetal Brain Female	brain
6	chr7:5873200-5896200	Weak transcription	Lung	lung
7	chr7:5875400-5896600	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr7:5876400-5896200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
9	chr7:5877400-5896200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
10	chr7:5878600-5898000	Weak transcription	Brain Angular Gyrus	brain
11	chr7:5882400-5896000	Weak transcription	Primary B cells from peripheral blood	blood
12	chr7:5882400-5896200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
13	chr7:5882400-5897600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
14	chr7:5882600-5896200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr7:5882800-5896800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
16	chr7:5882800-5896800	Weak transcription	Fetal Intestine Small	intestine
17	chr7:5883000-5897400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
18	chr7:5887800-5892200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
19	chr7:5887800-5895400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
20	chr7:5888000-5897600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr7:5888400-5893000	Strong transcription	Primary T cells from cord blood	blood
22	chr7:5889400-5896000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr7:5889600-5895800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
24	chr7:5889600-5896200	Weak transcription	Primary neutrophils fromperipheralblood	blood
25	chr7:5889800-5892000	Weak transcription	Primary monocytes fromperipheralblood	blood
26	chr7:5889800-5892200	Weak transcription	Monocytes-CD14+_RO01746	blood
27	chr7:5889800-5900600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr7:5890000-5924600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
29	chr7:5890200-5892400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr7:5890200-5896200	Weak transcription	Primary T helper cells PMA-I stimulated	--
31	chr7:5890800-5896200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
32	chr7:5891200-5896000	Weak transcription	Primary T cells fromperipheralblood	blood
33	chr7:5891400-5896600	Weak transcription	Primary T helper cells fromperipheralblood	blood
34	chr7:5891800-5892000	Enhancers	Cortex derived primary cultured neurospheres	brain
35	chr7:5892200-5892600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr7:5892200-5893000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
37	chr7:5892400-5892600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr7:5893000-5894600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
39	chr7:5893000-5894800	Weak transcription	Primary T cells from cord blood	blood
40	chr7:5894400-5894600	Enhancers	Duodenum Mucosa	Duodenum
41	chr7:5894600-5901400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
42	chr7:5894800-5895400	Strong transcription	Primary T cells from cord blood	blood
43	chr7:5894800-5896600	Weak transcription	Duodenum Mucosa	Duodenum
44	chr7:5895400-5897400	Weak transcription	Primary T cells from cord blood	blood
45	chr7:5895400-5938000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
46	chr7:5895800-5896600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
47	chr7:5896000-5896400	Enhancers	Primary B cells from peripheral blood	blood
48	chr7:5896000-5896800	Active TSS	Hela-S3	cervix
49	chr7:5896000-5899200	Enhancers	Primary T cells fromperipheralblood	blood
50	chr7:5896200-5896400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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