Variant report

Variant	esv2762643
Chromosome Location	chr7:5172994-5216265
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	ARID3A	chr7:5179826-5179837	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:5214192-5214521	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:5214184-5214495	K562	blood:	n/a	n/a
4	ATF3	chr7:5184097-5184376	K562	blood:	n/a	n/a
5	BACH1	chr7:5214153-5214316	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr7:5200590-5200642	GM12878	blood:	n/a	n/a
7	BHLHE40	chr7:5214113-5214362	K562	blood:	n/a	n/a
8	BHLHE40	chr7:5184107-5184335	K562	blood:	n/a	n/a
9	BHLHE40	chr7:5183971-5184469	GM12878	blood:	n/a	n/a
10	CBX3	chr7:5195797-5196160	K562	blood:	n/a	n/a
11	CEBPB	chr7:5181344-5181705	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr7:5181318-5181631	ECC-1	luminal epithelium:	n/a	n/a
13	CEBPB	chr7:5181298-5181610	K562	blood:	n/a	n/a
14	CEBPB	chr7:5173205-5173253	A549	lung:	n/a	n/a
15	CEBPB	chr7:5181506-5181536	IMR90	lung:	n/a	n/a
16	CEBPB	chr7:5213110-5213364	K562	blood:	n/a	chr7:5213237-5213248
17	CEBPB	chr7:5181401-5181600	K562	blood:	n/a	n/a
18	CEBPB	chr7:5201107-5201244	HepG2	liver:	n/a	n/a
19	CEBPB	chr7:5181333-5181706	K562	blood:	n/a	n/a
20	CEBPB	chr7:5213177-5213366	A549	lung:	n/a	chr7:5213237-5213248
21	CEBPB	chr7:5213178-5213296	HepG2	liver:	n/a	chr7:5213237-5213248
22	CEBPB	chr7:5213238-5213282	IMR90	lung:	n/a	n/a
23	CHD2	chr7:5214254-5214345	HepG2	liver:	n/a	n/a
24	CHD2	chr7:5184054-5184470	GM12878	blood:	n/a	n/a
25	CHD2	chr7:5200592-5200776	GM12878	blood:	n/a	n/a
26	CREB1	chr7:5183933-5184524	GM12878	blood:	n/a	n/a
27	CTCF	chr7:5195940-5196014	GM10248	blood:	n/a	n/a
28	CTCF	chr7:5214260-5214410	WERI-Rb-1	eye:	n/a	chr7:5214351-5214369 chr7:5214346-5214367
29	CTCF	chr7:5214260-5214410	HRPEpiC	eye:	n/a	chr7:5214351-5214369 chr7:5214346-5214367
30	CTCF	chr7:5179740-5179890	AG04449	skin:	n/a	chr7:5179807-5179828 chr7:5179805-5179823 chr7:5179806-5179822 chr7:5179808-5179821
31	CTCF	chr7:5214260-5214410	HL-60	blood:	n/a	chr7:5214351-5214369 chr7:5214346-5214367
32	CTCF	chr7:5214240-5214390	GM12869	blood:	n/a	chr7:5214351-5214369 chr7:5214346-5214367
33	CTCF	chr7:5179640-5179790	GM12866	blood:	n/a	n/a
34	CTCF	chr7:5179700-5179850	HCT-116	colon:	n/a	chr7:5179807-5179828 chr7:5179805-5179823 chr7:5179806-5179822 chr7:5179808-5179821
35	CTCF	chr7:5214205-5214436	SK-N-SH_RA	brain:	n/a	chr7:5214351-5214369 chr7:5214221-5214229 chr7:5214346-5214367
36	CTCF	chr7:5195892-5196041	GM12891	blood:	n/a	n/a
37	CTCF	chr7:5179635-5180058	MCF-7	breast:	n/a	chr7:5179807-5179828 chr7:5179912-5179930 chr7:5179805-5179823 chr7:5179806-5179822 chr7:5179808-5179821 chr7:5179915-5179928
38	CTCF	chr7:5214220-5214370	HEEpiC	esophagus:	n/a	chr7:5214351-5214369 chr7:5214221-5214229 chr7:5214346-5214367
39	CTCF	chr7:5214240-5214390	GM12867	blood:	n/a	chr7:5214351-5214369 chr7:5214346-5214367
40	CTCF	chr7:5179720-5179870	GM12864	blood:	n/a	chr7:5179807-5179828 chr7:5179805-5179823 chr7:5179806-5179822 chr7:5179808-5179821
41	CTCF	chr7:5200480-5200630	GM12864	blood:	n/a	n/a
42	CTCF	chr7:5214267-5214419	Lung_OC	lung:	n/a	chr7:5214351-5214369 chr7:5214346-5214367
43	CTCF	chr7:5179564-5179945	A549	lung:	n/a	chr7:5179807-5179828 chr7:5179912-5179930 chr7:5179805-5179823 chr7:5179806-5179822 chr7:5179808-5179821 chr7:5179915-5179928
44	CTCF	chr7:5214000-5214150	HEK293	kidney:	n/a	n/a
45	CTCF	chr7:5179760-5179910	AG09309	skin:	n/a	chr7:5179807-5179828 chr7:5179805-5179823 chr7:5179806-5179822 chr7:5179808-5179821
46	CTCF	chr7:5179719-5179935	H1-hESC	embryonic stem cell:	n/a	chr7:5179807-5179828 chr7:5179912-5179930 chr7:5179805-5179823 chr7:5179806-5179822 chr7:5179808-5179821 chr7:5179915-5179928
47	CTCF	chr7:5184311-5184428	GM19238	blood:	n/a	n/a
48	CTCF	chr7:5214240-5214390	RPTEC	kidney:	n/a	chr7:5214351-5214369 chr7:5214346-5214367
49	CTCF	chr7:5214280-5214430	HVMF	connective:	n/a	chr7:5214351-5214369 chr7:5214346-5214367
50	CTCF	chr7:5214268-5214452	HepG2	liver:	n/a	chr7:5214351-5214369 chr7:5214346-5214367

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:5184295-5184345	Hela-S3	cervix:	n/a
2	chr7:5184155-5184205	GM12878	blood:	n/a
3	chr7:5184295-5184345	Hela-S3	cervix:	n/a
4	chr7:5184155-5184205	GM12878	blood:	n/a
5	chr7:5183992-5184042	AG10803	skin:	n/a
6	chr7:5179884-5179934	BE2_C	brain:	n/a
7	chr7:5184155-5184205	AG10803	skin:	n/a
8	chr7:5184536-5184586	HCT-116	colon:	n/a
9	chr7:5183992-5184042	AG04449	skin:	fetal
10	chr7:5186528-5186578	U87	brain:	n/a
11	chr7:5179884-5179934	HIPEpiC	eye:	n/a
12	chr7:5184295-5184345	NH-A	brain:	n/a
13	chr7:5184014-5184064	AoSMC	blood vessel:	n/a
14	chr7:5184155-5184205	SAEC	small airway:	n/a
15	chr7:5186528-5186578	T-47D	breast:	n/a
16	chr7:5184014-5184064	NHBE	bronchial:	n/a
17	chr7:5179884-5179934	T-47D	breast:	n/a
18	chr7:5184295-5184345	HepG2	liver:	n/a
19	chr7:5184155-5184205	K562	blood:	n/a
20	chr7:5183992-5184042	AG09309	skin:	n/a
21	chr7:5186528-5186578	HepG2	liver:	n/a
22	chr7:5184295-5184345	K562	blood:	n/a
23	chr7:5184155-5184205	NHBE	bronchial:	n/a
24	chr7:5184155-5184205	BJ	skin:	n/a
25	chr7:5184014-5184064	AG04450	lung:	fetal
26	chr7:5184536-5184586	SK-N-MC	brain:	n/a
27	chr7:5184155-5184205	LNCaP	prostate:	n/a
28	chr7:5184155-5184205	NT2-D1	testis:	n/a
29	chr7:5183992-5184042	SK-N-MC	brain:	n/a
30	chr7:5179884-5179934	IMR90	lung:	fetal
31	chr7:5179884-5179934	PFSK-1	brain:	n/a
32	chr7:5184155-5184205	ovcar-3	ovarian:	n/a
33	chr7:5184295-5184345	BJ	skin:	n/a
34	chr7:5184295-5184345	GM19239	blood:	n/a
35	chr7:5184536-5184586	ovcar-3	ovarian:	n/a
36	chr7:5186528-5186578	AG09319	gingival:	n/a
37	chr7:5184295-5184345	ECC-1	luminal epithelium:	n/a
38	chr7:5184155-5184205	HEEpiC	esophagus:	n/a
39	chr7:5179884-5179934	Jurkat	blood:	n/a
40	chr7:5184155-5184205	HUVEC	blood vessel:	n/a
41	chr7:5184014-5184064	GM06990	blood:	n/a
42	chr7:5186528-5186578	LNCaP	prostate:	n/a
43	chr7:5184536-5184586	PANC-1	pancreas:	n/a
44	chr7:5186528-5186578	HEEpiC	esophagus:	n/a
45	chr7:5184295-5184345	HRE	kidney:	n/a
46	chr7:5179884-5179934	AG04450	lung:	fetal
47	chr7:5184536-5184586	HCPEpiC	choroid plexus:	n/a
48	chr7:5179884-5179934	HL-60	blood:	n/a
49	chr7:5184014-5184064	IMR90	lung:	fetal
50	chr7:5183992-5184042	PFSK-1	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:5198471..5200829-chr7:5846767..5848341,2	MCF-7	breast:
2	chr7:5214098..5214806-chr7:5527508..5528054,2	MCF-7	breast:
3	chr7:5195253..5196797-chr7:5849975..5851503,2	MCF-7	breast:
4	chr7:5184212..5184729-chr7:5862163..5863064,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MMD2-3	chr7:5183878-5184177	NR_034163
2	lnc-MMD2-3	chr7:5176186-5176320	NR_034163

Variant related genes	Relation type
RNU6-215P	TF binding region
ZNF890P	TF binding region
RNU6-215P	CpG island
ZNF890P	CpG island
ENSG00000235944	chromatin interactions

Extended variants
information (count: 2168 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:2168 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs564562002	chr7:5173000-5173001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs181246021	chr7:5173027-5173028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs62441995	chr7:5173045-5173046	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs369296683	chr7:5173050-5173051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs544389907	chr7:5173074-5173075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs115124575	chr7:5173080-5173081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs111564184	chr7:5173107-5173108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs186123451	chr7:5173119-5173120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs62441996	chr7:5173155-5173156	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs559893023	chr7:5173176-5173177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs530087639	chr7:5173195-5173196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs113732347	chr7:5173202-5173203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs551890208	chr7:5173209-5173210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs111360182	chr7:5173212-5173213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs376999670	chr7:5173288-5173289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs112844843	chr7:5173294-5173295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs62441997	chr7:5173310-5173311	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs570711574	chr7:5173336-5173337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs535388546	chr7:5173337-5173338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs538393217	chr7:5173344-5173345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs386709683	chr7:5173360-5173361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs73057815	chr7:5173361-5173362	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs539826602	chr7:5173362-5173363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs376881339	chr7:5173390-5173391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs568141231	chr7:5173391-5173392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs386709684	chr7:5173414-5173415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs111348699	chr7:5173429-5173430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs572045035	chr7:5173438-5173439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs574128683	chr7:5173487-5173488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs13245845	chr7:5173492-5173493	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs62441998	chr7:5173499-5173500	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs527319350	chr7:5173502-5173503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs545418100	chr7:5173535-5173536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs563707320	chr7:5173573-5173574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs531316183	chr7:5173601-5173602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs576197970	chr7:5173605-5173606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs568211454	chr7:5173611-5173612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs375515596	chr7:5173614-5173615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs369638010	chr7:5173627-5173628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs374253808	chr7:5173652-5173653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs115605612	chr7:5173691-5173692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs539715520	chr7:5173696-5173697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs111706653	chr7:5173699-5173700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs570024000	chr7:5173710-5173711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs543602064	chr7:5173791-5173792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs537543806	chr7:5173830-5173831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs187567449	chr7:5173831-5173832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs139419878	chr7:5173873-5173874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs9691981	chr7:5173883-5173884	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs374961106	chr7:5173930-5173931	Weak transcription	n/a	n/a	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
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	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
Glioblastoma multiforme	21525872	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
Pancreatic cancer	17952125	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:207 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:5171400-5180400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
2	chr7:5179800-5180000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
3	chr7:5179800-5180000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
4	chr7:5179800-5180000	Weak transcription	Primary T helper cells fromperipheralblood	blood
5	chr7:5179800-5180600	Enhancers	Primary T killer memory cells from peripheral blood	blood
6	chr7:5180000-5180200	Enhancers	Primary T helper cells fromperipheralblood	blood
7	chr7:5180000-5182200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
8	chr7:5180000-5182200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
9	chr7:5180200-5180800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr7:5180200-5182800	Weak transcription	Primary T helper cells fromperipheralblood	blood
11	chr7:5180400-5180600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
12	chr7:5180600-5181800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
13	chr7:5180600-5183200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
14	chr7:5180800-5183800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr7:5181400-5181600	Enhancers	Primary T helper cells PMA-I stimulated	--
16	chr7:5181600-5182400	Enhancers	Fetal Thymus	thymus
17	chr7:5181600-5182800	Weak transcription	Primary T helper cells PMA-I stimulated	--
18	chr7:5181800-5183000	Enhancers	Primary T killer memory cells from peripheral blood	blood
19	chr7:5182000-5182800	Enhancers	Primary T helper naive cells from peripheral blood	blood
20	chr7:5182200-5182800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
21	chr7:5182200-5183800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
22	chr7:5182400-5182600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
23	chr7:5182400-5183400	Weak transcription	Fetal Thymus	thymus
24	chr7:5182600-5183000	Flanking Active TSS	Primary T cells fromperipheralblood	blood
25	chr7:5182600-5183200	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
26	chr7:5182800-5183200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
27	chr7:5182800-5183200	Active TSS	Primary T helper naive cells from peripheral blood	blood
28	chr7:5182800-5183200	Active TSS	Primary T helper cells fromperipheralblood	blood
29	chr7:5182800-5183400	Enhancers	Primary T cells from cord blood	blood
30	chr7:5182800-5183400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
31	chr7:5182800-5184000	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
32	chr7:5182800-5184000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
33	chr7:5182800-5184200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
34	chr7:5182800-5184600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
35	chr7:5183000-5183400	Bivalent/Poised TSS	Primary T cells fromperipheralblood	blood
36	chr7:5183000-5183400	Active TSS	Primary T killer memory cells from peripheral blood	blood
37	chr7:5183200-5183400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
38	chr7:5183200-5183400	Active TSS	Primary T regulatory cells fromperipheralblood	blood
39	chr7:5183200-5183600	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
40	chr7:5183200-5184200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
41	chr7:5183200-5184200	Active TSS	Primary T killer naive cells fromperipheralblood	blood
42	chr7:5183400-5183600	Flanking Active TSS	Primary T cells from cord blood	blood
43	chr7:5183400-5183600	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
44	chr7:5183400-5183600	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
45	chr7:5183400-5183600	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
46	chr7:5183400-5183800	Enhancers	Primary B cells from peripheral blood	blood
47	chr7:5183400-5183800	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
48	chr7:5183400-5183800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr7:5183400-5183800	Enhancers	Fetal Thymus	thymus
50	chr7:5183400-5183800	Enhancers	GM12878-XiMat	blood

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