Variant report

Variant	nsv1024675
Chromosome Location	chr7:5868561-5965441
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1073)
CpG islands
(count:1653)
Chromatin interactive
region (count:10)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1073 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

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	chr7:5938735-5938983	GM12878	blood:	n/a	n/a
3	BATF	chr7:5938176-5938390	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	chr7:5896140-5896326	GM12878	blood:	n/a	n/a
9	BHLHE40	chr7:5889190-5889204	K562	blood:	n/a	n/a
10	BHLHE40	chr7:5938233-5938412	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	chr7:5938092-5938432	K562	blood:	n/a	n/a
14	CBX3	chr7:5937356-5938688	K562	blood:	n/a	n/a
15	CBX3	chr7:5938925-5939374	K562	blood:	n/a	n/a
16	CEBPB	chr7:5891809-5891870	IMR90	lung:	n/a	n/a
17	CEBPB	chr7:5892977-5893179	IMR90	lung:	n/a	chr7:5893027-5893038
18	CEBPB	chr7:5892975-5893180	HepG2	liver:	n/a	chr7:5893027-5893038
19	CEBPB	chr7:5890537-5890700	A549	lung:	n/a	chr7:5890571-5890582
20	CEBPB	chr7:5893018-5893091	Hela-S3	cervix:	n/a	chr7:5893027-5893038
21	CEBPB	chr7:5892955-5893172	K562	blood:	n/a	chr7:5893027-5893038
22	CEBPB	chr7:5912087-5912368	IMR90	lung:	n/a	n/a
23	CEBPB	chr7:5890492-5890732	K562	blood:	n/a	chr7:5890571-5890582
24	CEBPB	chr7:5892913-5893127	H1-hESC	embryonic stem cell:	n/a	chr7:5893027-5893038
25	CEBPB	chr7:5929893-5930182	K562	blood:	n/a	n/a
26	CEBPB	chr7:5896180-5896389	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr7:5891846-5891857	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr7:5872011-5872190	K562	blood:	n/a	n/a
29	CEBPB	chr7:5890535-5890604	H1-hESC	embryonic stem cell:	n/a	chr7:5890571-5890582
30	CEBPB	chr7:5890460-5890688	HepG2	liver:	n/a	chr7:5890571-5890582
31	CEBPB	chr7:5929312-5929450	IMR90	lung:	n/a	n/a
32	CEBPB	chr7:5892975-5893174	A549	lung:	n/a	chr7:5893027-5893038
33	CEBPB	chr7:5872758-5872976	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr7:5942532-5942815	K562	blood:	n/a	chr7:5942734-5942743 chr7:5942734-5942745
35	CEBPB	chr7:5890537-5890656	IMR90	lung:	n/a	chr7:5890571-5890582
36	CHD2	chr7:5894459-5894465	HepG2	liver:	n/a	n/a
37	CHD2	chr7:5938146-5938417	Hela-S3	cervix:	n/a	n/a
38	CREB1	chr7:5938052-5938355	HepG2	liver:	n/a	n/a
39	CREB1	chr7:5938058-5938399	A549	lung:	n/a	n/a
40	CTCF	chr7:5939259-5939394	MCF-7	breast:	n/a	n/a
41	CTCF	chr7:5880420-5880570	MCF-7	breast:	n/a	chr7:5880500-5880513 chr7:5880497-5880515
42	CTCF	chr7:5938188-5938377	MCF-7	breast:	n/a	chr7:5938264-5938273
43	CTCF	chr7:5938216-5938380	HUVEC	blood vessel:	n/a	chr7:5938264-5938273
44	CTCF	chr7:5905080-5905144	GM12892	blood:	n/a	n/a
45	CTCF	chr7:5908780-5908930	A549	lung:	n/a	chr7:5908846-5908864 chr7:5908849-5908862
46	CTCF	chr7:5905063-5905135	Medullo	brain:	n/a	n/a
47	CTCF	chr7:5896100-5896250	GM12866	blood:	n/a	n/a
48	CTCF	chr7:5905000-5905150	NB4	blood:	n/a	n/a
49	CTCF	chr7:5877589-5877607	Spleen_OC	spleen:	n/a	n/a
50	CTCF	chr7:5896240-5896390	GM12865	blood:	n/a	n/a

(count:1653 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:5911701-5911751	BJ	skin:	n/a
2	chr7:5935002-5935052	AG09319	gingival:	n/a
3	chr7:5938195-5938245	PFSK-1	brain:	n/a
4	chr7:5890037-5890087	GM12878	blood:	n/a
5	chr7:5887023-5887073	AG04449	skin:	fetal
6	chr7:5938293-5938343	AG10803	skin:	n/a
7	chr7:5911701-5911751	BJ	skin:	n/a
8	chr7:5935002-5935052	AG09319	gingival:	n/a
9	chr7:5938195-5938245	PFSK-1	brain:	n/a
10	chr7:5890037-5890087	GM12878	blood:	n/a
11	chr7:5887023-5887073	AG04449	skin:	fetal
12	chr7:5938293-5938343	AG10803	skin:	n/a
13	chr7:5938195-5938245	T-47D	breast:	n/a
14	chr7:5935002-5935052	HAEpiC	amniotic membrane:	n/a
15	chr7:5890037-5890087	A549	lung:	n/a
16	chr7:5886722-5886772	HUVEC	blood vessel:	n/a
17	chr7:5938193-5938243	Jurkat	blood:	n/a
18	chr7:5941157-5941207	AG04450	lung:	fetal
19	chr7:5937486-5937536	HL-60	blood:	n/a
20	chr7:5938288-5938338	AG04449	skin:	fetal
21	chr7:5938204-5938254	SK-N-SH	brain:	n/a
22	chr7:5938193-5938243	GM12892	blood:	n/a
23	chr7:5938288-5938338	SK-N-SH	brain:	n/a
24	chr7:5920535-5920585	SAEC	small airway:	n/a
25	chr7:5920535-5920585	HRCEpiC	kidney:	n/a
26	chr7:5883645-5883695	HRCEpiC	kidney:	n/a
27	chr7:5890037-5890087	AG04450	lung:	fetal
28	chr7:5911701-5911751	HAEpiC	amniotic membrane:	n/a
29	chr7:5938204-5938254	AoSMC	blood vessel:	n/a
30	chr7:5911701-5911751	A549	lung:	n/a
31	chr7:5939791-5939841	GM06990	blood:	n/a
32	chr7:5937433-5937483	IMR90	lung:	fetal
33	chr7:5938195-5938245	GM06990	blood:	n/a
34	chr7:5938195-5938245	GM12891	blood:	n/a
35	chr7:5911800-5911850	HCM	heart:	n/a
36	chr7:5935002-5935052	AoSMC	blood vessel:	n/a
37	chr7:5938195-5938245	NT2-D1	testis:	n/a
38	chr7:5919583-5919633	HUVEC	blood vessel:	n/a
39	chr7:5938204-5938254	HepG2	liver:	n/a
40	chr7:5963438-5963488	A549	lung:	n/a
41	chr7:5883645-5883695	HNPCEpiC	eye:	n/a
42	chr7:5935002-5935052	HRCEpiC	kidney:	n/a
43	chr7:5885244-5885294	GM06990	blood:	n/a
44	chr7:5939791-5939841	MCF-7	breast:	n/a
45	chr7:5937433-5937483	ECC-1	luminal epithelium:	n/a
46	chr7:5938193-5938243	Hepatocyte	liver:	n/a
47	chr7:5938227-5938277	BE2_C	brain:	n/a
48	chr7:5938193-5938243	NT2-D1	testis:	n/a
49	chr7:5935002-5935052	ECC-1	luminal epithelium:	n/a
50	chr7:5911701-5911751	AG10803	skin:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:5875724..5878623-chr7:5880700..5882793,2	MCF-7	breast:
2	chr7:5875724..5878623-chr7:5880700..5882793,2	MCF-7	breast:
3	chr7:5921888..5923776-chr7:6615172..6617060,2	K562	blood:
4	chr7:5877107..5878733-chr7:5880762..5883645,2	K562	blood:
5	chr7:5877192..5879014-chr7:6172405..6175361,2	K562	blood:
6	chr7:5877107..5878733-chr7:5880762..5883645,2	K562	blood:
7	chr7:5895754..5896691-chr7:6036473..6037181,2	MCF-7	breast:
8	chr7:5866466..5869217-chr7:5871734..5873608,2	MCF-7	breast:
9	chr7:5866466..5869217-chr7:5871734..5873608,2	MCF-7	breast:
10	chr7:5896217..5898583-chr7:97641356..97642858,2	MCF-7	breast:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OCM-2	chr7:5965263-5965571	NONHSAT118958
2	lnc-OCM-3	chr7:5880321-5880487	NONHSAT118944
3	lnc-OCM-3	chr7:5878701-5878783	NONHSAT118942
4	lnc-RSPH10B-1	chr7:5911384-5911681	NONHSAT118956
5	lnc-OCM-3	chr7:5873158-5873199	NONHSAT118944
6	lnc-OCM-3	chr7:5873158-5873199	NONHSAT118942
7	lnc-OCM-3	chr7:5870812-5870914	NONHSAT118942
8	lnc-OCM-3	chr7:5893738-5893857	NONHSAT118944
9	lnc-OCM-3	chr7:5873158-5873199	NONHSAT118948
10	lnc-OCM-2	chr7:5964372-5964445	NONHSAT118958
11	lnc-OCM-3	chr7:5879580-5879706	NONHSAT118944
12	lnc-OCM-3	chr7:5878820-5878850	NONHSAT118948

No data

Variant related genes	Relation type
CCZ1	TF binding region
OCM	TF binding region
ZNF815P	TF binding region
RN7SL556P	TF binding region
CCZ1	CpG island
OCM	CpG island
ZNF815P	CpG island
RN7SL556P	CpG island

Extended variants
information (count: 5522 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:5522 , 50 per page) page: 1 2 3 4 5 6 7 ... 111

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12537672	chr7:5868561-5868562	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs574298863	chr7:5868597-5868598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs539934538	chr7:5868658-5868659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs56696175	chr7:5868662-5868663	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs557391481	chr7:5868667-5868668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs527390397	chr7:5868696-5868697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs545824495	chr7:5868697-5868698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs10264756	chr7:5868751-5868752	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs564211745	chr7:5868789-5868790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs575736916	chr7:5868804-5868805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs531162563	chr7:5868823-5868824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs370400280	chr7:5868840-5868841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs186990836	chr7:5868867-5868868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs567980744	chr7:5868876-5868877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs529122405	chr7:5868894-5868895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs547256247	chr7:5868910-5868911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs72030051	chr7:5868922-5868923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs386409434	chr7:5868945-5868946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs190536768	chr7:5868959-5868960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs539544885	chr7:5868993-5868994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs181335010	chr7:5869024-5869025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs570084479	chr7:5869029-5869030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs537404866	chr7:5869098-5869099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs151163645	chr7:5869110-5869111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs28387061	chr7:5869115-5869116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs530264586	chr7:5869166-5869167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs574364352	chr7:5869185-5869186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs541656267	chr7:5869199-5869200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs553281079	chr7:5869210-5869211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs185646667	chr7:5869239-5869240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs117284830	chr7:5869252-5869253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs555181816	chr7:5869254-5869255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs549068295	chr7:5869293-5869294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs140230610	chr7:5869294-5869295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs531223591	chr7:5869318-5869319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs114910522	chr7:5869346-5869347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs13234949	chr7:5869363-5869364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs144964965	chr7:5869364-5869365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs55745170	chr7:5869367-5869368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs2161014	chr7:5869368-5869369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs115705875	chr7:5869370-5869371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs561677633	chr7:5869412-5869413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs529172685	chr7:5869420-5869421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs547613370	chr7:5869424-5869425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs189965139	chr7:5869458-5869459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs372575256	chr7:5869527-5869528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs138876345	chr7:5869550-5869551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs570147182	chr7:5869565-5869566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs537468403	chr7:5869609-5869610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs116473068	chr7:5869616-5869617	Weak 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
Pancreatic cancer	17952125	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:1141 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:5863400-5870600	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr7:5863600-5870800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr7:5863600-5874200	Weak transcription	Thymus	Thymus
4	chr7:5863600-5896800	Weak transcription	Esophagus	oesophagus
5	chr7:5863800-5870600	Weak transcription	Fetal Brain Female	brain
6	chr7:5863800-5871000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr7:5863800-5879200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr7:5863800-5881600	Weak transcription	Fetal Intestine Small	intestine
9	chr7:5863800-5887000	Weak transcription	Primary B cells from cord blood	blood
10	chr7:5863800-5891400	Weak transcription	Liver	Liver
11	chr7:5863800-5891400	Weak transcription	Brain Hippocampus Middle	brain
12	chr7:5863800-5896200	Weak transcription	Adipose Nuclei	Adipose
13	chr7:5864000-5870800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
14	chr7:5864000-5880400	Weak transcription	Brain Substantia Nigra	brain
15	chr7:5864200-5870600	Weak transcription	Monocytes-CD14+_RO01746	blood
16	chr7:5864200-5870800	Weak transcription	Primary monocytes fromperipheralblood	blood
17	chr7:5864200-5871000	Weak transcription	Spleen	Spleen
18	chr7:5864200-5873000	Weak transcription	HepG2	liver
19	chr7:5864200-5873200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr7:5864200-5880400	Weak transcription	Primary B cells from peripheral blood	blood
21	chr7:5864200-5893600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
22	chr7:5864400-5870600	Weak transcription	Primary neutrophils fromperipheralblood	blood
23	chr7:5864600-5872200	Weak transcription	Primary T cells from cord blood	blood
24	chr7:5864800-5870000	Weak transcription	Fetal Brain Male	brain
25	chr7:5864800-5870800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr7:5864800-5872600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
27	chr7:5865600-5872600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
28	chr7:5867000-5870400	Weak transcription	NH-A	brain
29	chr7:5867400-5870800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
30	chr7:5867600-5870200	Weak transcription	Primary T cells fromperipheralblood	blood
31	chr7:5867600-5885000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
32	chr7:5867800-5870200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
33	chr7:5867800-5870400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
34	chr7:5867800-5870600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
35	chr7:5867800-5870800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
36	chr7:5867800-5871000	Weak transcription	Primary T helper cells PMA-I stimulated	--
37	chr7:5868000-5870600	Weak transcription	Primary T helper cells fromperipheralblood	blood
38	chr7:5869200-5881600	Weak transcription	Fetal Stomach	stomach
39	chr7:5870000-5871200	Enhancers	Fetal Brain Male	brain
40	chr7:5870000-5871600	Enhancers	Cortex derived primary cultured neurospheres	brain
41	chr7:5870200-5870400	Enhancers	Primary T cells fromperipheralblood	blood
42	chr7:5870200-5870600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr7:5870200-5871600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
44	chr7:5870400-5870600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr7:5870400-5870600	Enhancers	Fetal Kidney	kidney
46	chr7:5870400-5870600	Enhancers	NH-A	brain
47	chr7:5870400-5870800	Enhancers	Breast Myoepithelial Primary Cells	Breast
48	chr7:5870400-5871600	Genic enhancers	Primary T cells fromperipheralblood	blood
49	chr7:5870400-5871600	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
50	chr7:5870600-5870800	Enhancers	Fetal Brain Female	brain

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