Variant report

Variant	esv1804099
Chromosome Location	chr7:5883522-5913393
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:382)
CpG islands
(count:551)
Chromatin interactive
region (count:3)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:382 , 50 per page) page: 1 2 3 4 5 6 7 8

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	chr7:5891809-5891870	IMR90	lung:	n/a	n/a
8	CEBPB	chr7:5892975-5893174	A549	lung:	n/a	chr7:5893027-5893038
9	CEBPB	chr7:5896180-5896389	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr7:5892913-5893127	H1-hESC	embryonic stem cell:	n/a	chr7:5893027-5893038
11	CEBPB	chr7:5892975-5893180	HepG2	liver:	n/a	chr7:5893027-5893038
12	CEBPB	chr7:5890535-5890604	H1-hESC	embryonic stem cell:	n/a	chr7:5890571-5890582
13	CEBPB	chr7:5893018-5893091	Hela-S3	cervix:	n/a	chr7:5893027-5893038
14	CEBPB	chr7:5912087-5912368	IMR90	lung:	n/a	n/a
15	CEBPB	chr7:5892977-5893179	IMR90	lung:	n/a	chr7:5893027-5893038
16	CEBPB	chr7:5890492-5890732	K562	blood:	n/a	chr7:5890571-5890582
17	CEBPB	chr7:5890537-5890700	A549	lung:	n/a	chr7:5890571-5890582
18	CEBPB	chr7:5890460-5890688	HepG2	liver:	n/a	chr7:5890571-5890582
19	CEBPB	chr7:5891846-5891857	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr7:5890537-5890656	IMR90	lung:	n/a	chr7:5890571-5890582
21	CEBPB	chr7:5892955-5893172	K562	blood:	n/a	chr7:5893027-5893038
22	CHD2	chr7:5894459-5894465	HepG2	liver:	n/a	n/a
23	CTCF	chr7:5896240-5896390	GM12864	blood:	n/a	n/a
24	CTCF	chr7:5908706-5908950	HepG2	liver:	n/a	chr7:5908846-5908864 chr7:5908849-5908862
25	CTCF	chr7:5896072-5896419	GM12878	blood:	n/a	n/a
26	CTCF	chr7:5896200-5896350	AG09309	skin:	n/a	n/a
27	CTCF	chr7:5896248-5896397	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr7:5896046-5896411	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr7:5896160-5896310	AG10803	skin:	n/a	n/a
30	CTCF	chr7:5896160-5896310	BJ	skin:	n/a	n/a
31	CTCF	chr7:5896280-5896430	NHDF-neo	bronchial:	n/a	n/a
32	CTCF	chr7:5896076-5896406	K562	blood:	n/a	n/a
33	CTCF	chr7:5896100-5896250	HMF	breast:	n/a	n/a
34	CTCF	chr7:5896154-5896403	Fibrobl	skin:	n/a	n/a
35	CTCF	chr7:5896160-5896310	HCT-116	colon:	n/a	n/a
36	CTCF	chr7:5896100-5896250	GM12866	blood:	n/a	n/a
37	CTCF	chr7:5896200-5896350	HCFaa	heart:	n/a	n/a
38	CTCF	chr7:5896180-5896330	GM12875	blood:	n/a	n/a
39	CTCF	chr7:5896100-5896250	WI-38	lung:	n/a	n/a
40	CTCF	chr7:5896200-5896350	HBMEC	blood vessel:	n/a	n/a
41	CTCF	chr7:5896139-5896374	A549	lung:	n/a	n/a
42	CTCF	chr7:5896060-5896210	HMEC	breast:	n/a	n/a
43	CTCF	chr7:5896143-5896404	MCF-7	breast:	n/a	n/a
44	CTCF	chr7:5896093-5896386	Pancreas_OC	pancreas:	n/a	n/a
45	CTCF	chr7:5896240-5896390	HFF-Myc	foreskin:	n/a	n/a
46	CTCF	chr7:5896013-5896549	K562	blood:	n/a	n/a
47	CTCF	chr7:5908800-5908950	NHEK	skin:	n/a	chr7:5908846-5908864 chr7:5908849-5908862
48	CTCF	chr7:5896040-5896190	HA-sp	spinal cord:	n/a	n/a
49	CTCF	chr7:5895910-5896008	GM19240	blood:	n/a	n/a
50	CTCF	chr7:5896100-5896250	HEEpiC	esophagus:	n/a	n/a

(count:551 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:5883645-5883695	ECC-1	luminal epithelium:	n/a
2	chr7:5885244-5885294	HUVEC	blood vessel:	n/a
3	chr7:5883645-5883695	ECC-1	luminal epithelium:	n/a
4	chr7:5885244-5885294	HUVEC	blood vessel:	n/a
5	chr7:5883645-5883695	AoSMC	blood vessel:	n/a
6	chr7:5911701-5911751	SKMC	muscle:	n/a
7	chr7:5911900-5911950	Hepatocyte	liver:	n/a
8	chr7:5883645-5883695	LNCaP	prostate:	n/a
9	chr7:5883645-5883695	NB4	blood:	n/a
10	chr7:5883645-5883695	SAEC	small airway:	n/a
11	chr7:5887023-5887073	HPAEpiC	pulmonary alveolar:	n/a
12	chr7:5888077-5888127	HL-60	blood:	n/a
13	chr7:5890037-5890087	BJ	skin:	n/a
14	chr7:5911701-5911751	ProgFib	skin:	n/a
15	chr7:5888077-5888127	HEK293	kidney:	embryo
16	chr7:5883645-5883695	ovcar-3	ovarian:	n/a
17	chr7:5886722-5886772	HCF	heart:	n/a
18	chr7:5911701-5911751	T-47D	breast:	n/a
19	chr7:5885244-5885294	HepG2	liver:	n/a
20	chr7:5911701-5911751	NHBE	bronchial:	n/a
21	chr7:5890037-5890087	HEK293	kidney:	embryo
22	chr7:5885244-5885294	HL-60	blood:	n/a
23	chr7:5911701-5911751	HepG2	liver:	n/a
24	chr7:5885244-5885294	GM12892	blood:	n/a
25	chr7:5911701-5911751	Hela-S3	cervix:	n/a
26	chr7:5887023-5887073	GM12878	blood:	n/a
27	chr7:5911900-5911950	HEEpiC	esophagus:	n/a
28	chr7:5885244-5885294	HCPEpiC	choroid plexus:	n/a
29	chr7:5890037-5890087	HNPCEpiC	eye:	n/a
30	chr7:5911701-5911751	HCT-116	colon:	n/a
31	chr7:5888077-5888127	HNPCEpiC	eye:	n/a
32	chr7:5887023-5887073	GM06990	blood:	n/a
33	chr7:5888077-5888127	NT2-D1	testis:	n/a
34	chr7:5887023-5887073	PANC-1	pancreas:	n/a
35	chr7:5887023-5887073	LNCaP	prostate:	n/a
36	chr7:5886722-5886772	HepG2	liver:	n/a
37	chr7:5886722-5886772	ProgFib	skin:	n/a
38	chr7:5888077-5888127	ECC-1	luminal epithelium:	n/a
39	chr7:5887023-5887073	AoSMC	blood vessel:	n/a
40	chr7:5883645-5883695	HPAEpiC	pulmonary alveolar:	n/a
41	chr7:5885244-5885294	GM12878	blood:	n/a
42	chr7:5885244-5885294	BE2_C	brain:	n/a
43	chr7:5885244-5885294	ECC-1	luminal epithelium:	n/a
44	chr7:5911900-5911950	HL-60	blood:	n/a
45	chr7:5888077-5888127	AG09309	skin:	n/a
46	chr7:5911701-5911751	HRE	kidney:	n/a
47	chr7:5887023-5887073	AG09309	skin:	n/a
48	chr7:5911900-5911950	Jurkat	blood:	n/a
49	chr7:5886722-5886772	GM12892	blood:	n/a
50	chr7:5911701-5911751	GM12878	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr7:5895754..5896691-chr7:6036473..6037181,2	MCF-7	breast:
2	chr7:5896217..5898583-chr7:97641356..97642858,2	MCF-7	breast:
3	chr7:5877107..5878733-chr7:5880762..5883645,2	K562	blood:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RSPH10B-1	chr7:5911384-5911681	NONHSAT118956
2	lnc-OCM-3	chr7:5893738-5893857	NONHSAT118944

No data

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

Extended variants
information (count: 1952 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:1952 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs308092	chr7:5883522-5883523	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs555881376	chr7:5883525-5883526	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs141137739	chr7:5883563-5883564	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs541062729	chr7:5883597-5883598	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs17135838	chr7:5883606-5883607	Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs533466950	chr7:5883645-5883646	Weak transcription Strong transcription Bivalent Enhancer	CpG island	1 gene(s)	Overlapped CNVs	n/a
7	rs546231102	chr7:5883666-5883667	Weak transcription Strong transcription Bivalent Enhancer	CpG island	1 gene(s)	Overlapped CNVs	n/a
8	rs563568637	chr7:5883678-5883679	Weak transcription Strong transcription Bivalent Enhancer	CpG island	1 gene(s)	Overlapped CNVs	n/a
9	rs567815263	chr7:5883696-5883697	Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs561711795	chr7:5883702-5883703	Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs568060969	chr7:5883722-5883723	Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs528938512	chr7:5883723-5883724	Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs182888071	chr7:5883740-5883741	Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs35132962	chr7:5883768-5883769	Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs397767037	chr7:5883782-5883783	Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs201660548	chr7:5883783-5883784	Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs565638302	chr7:5883788-5883789	Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs539762336	chr7:5883820-5883821	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs186598143	chr7:5883821-5883822	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs529102037	chr7:5883827-5883828	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs368120511	chr7:5883831-5883832	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs386709783	chr7:5883839-5883840	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs111970190	chr7:5883841-5883842	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs56066846	chr7:5883860-5883861	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs541474403	chr7:5883868-5883869	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs553107533	chr7:5883889-5883890	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs577948491	chr7:5883900-5883901	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs308091	chr7:5883905-5883906	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs571878879	chr7:5883926-5883927	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs28694105	chr7:5883935-5883936	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs66472645	chr7:5883949-5883950	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs563471039	chr7:5883953-5883954	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs531057821	chr7:5883954-5883955	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs367656652	chr7:5883959-5883960	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs308090	chr7:5883965-5883966	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs561494811	chr7:5883979-5883980	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs28412201	chr7:5883987-5883988	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs547438765	chr7:5883994-5883995	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs565565102	chr7:5884009-5884010	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs189200081	chr7:5884018-5884019	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs551738881	chr7:5884024-5884025	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs555464784	chr7:5884044-5884045	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs569962011	chr7:5884072-5884073	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs35151193	chr7:5884087-5884088	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs537294909	chr7:5884123-5884124	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs370731059	chr7:5884132-5884133	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs376842538	chr7:5884144-5884145	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs369566165	chr7:5884147-5884148	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs553416991	chr7:5884207-5884208	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs577657264	chr7:5884211-5884212	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

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

Chromatin state (count:223 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:5863600-5896800	Weak transcription	Esophagus	oesophagus
2	chr7:5863800-5887000	Weak transcription	Primary B cells from cord blood	blood
3	chr7:5863800-5891400	Weak transcription	Liver	Liver
4	chr7:5863800-5891400	Weak transcription	Brain Hippocampus Middle	brain
5	chr7:5863800-5896200	Weak transcription	Adipose Nuclei	Adipose
6	chr7:5864200-5893600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr7:5867600-5885000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr7:5871400-5890600	Weak transcription	Brain Germinal Matrix	brain
9	chr7:5871400-5904600	Weak transcription	Spleen	Spleen
10	chr7:5871600-5889200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr7:5871600-5891800	Weak transcription	Cortex derived primary cultured neurospheres	brain
12	chr7:5871600-5896400	Weak transcription	Fetal Brain Female	brain
13	chr7:5873200-5896200	Weak transcription	Lung	lung
14	chr7:5875400-5896600	Weak transcription	Brain Inferior Temporal Lobe	brain
15	chr7:5876400-5896200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
16	chr7:5877400-5896200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
17	chr7:5877600-5891400	Weak transcription	Brain Cingulate Gyrus	brain
18	chr7:5878200-5888200	Weak transcription	Sigmoid Colon	Sigmoid Colon
19	chr7:5878400-5886800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
20	chr7:5878600-5885400	Strong transcription	Monocytes-CD14+_RO01746	blood
21	chr7:5878600-5885600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
22	chr7:5878600-5898000	Weak transcription	Brain Angular Gyrus	brain
23	chr7:5878800-5889600	Strong transcription	Primary neutrophils fromperipheralblood	blood
24	chr7:5879000-5884600	Weak transcription	Brain Anterior Caudate	brain
25	chr7:5879200-5886200	Strong transcription	Primary T helper cells fromperipheralblood	blood
26	chr7:5879200-5886600	Strong transcription	Primary T cells fromperipheralblood	blood
27	chr7:5880800-5885200	Strong transcription	Primary T helper cells PMA-I stimulated	--
28	chr7:5881200-5883600	Strong transcription	Primary monocytes fromperipheralblood	blood
29	chr7:5881600-5885000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr7:5881600-5886000	Strong transcription	Primary T cells from cord blood	blood
31	chr7:5881800-5885600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
32	chr7:5882000-5890800	Weak transcription	Fetal Stomach	stomach
33	chr7:5882200-5890800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
34	chr7:5882400-5888400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr7:5882400-5896000	Weak transcription	Primary B cells from peripheral blood	blood
36	chr7:5882400-5896200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
37	chr7:5882400-5897600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
38	chr7:5882600-5896200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr7:5882800-5896800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
40	chr7:5882800-5896800	Weak transcription	Fetal Intestine Small	intestine
41	chr7:5883000-5889000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
42	chr7:5883000-5897400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
43	chr7:5883600-5883800	Bivalent Enhancer	Muscle Satellite Cultured Cells	--
44	chr7:5883600-5884400	Weak transcription	Primary monocytes fromperipheralblood	blood
45	chr7:5884000-5888000	Weak transcription	Stomach Smooth Muscle	stomach
46	chr7:5884400-5889800	Strong transcription	Primary monocytes fromperipheralblood	blood
47	chr7:5884600-5885400	Strong transcription	Brain Anterior Caudate	brain
48	chr7:5885000-5888000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
49	chr7:5885200-5888800	Weak transcription	Primary T helper cells PMA-I stimulated	--
50	chr7:5885400-5886400	Weak transcription	Monocytes-CD14+_RO01746	blood

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