Variant report

Variant	nsv497792
Chromosome Location	chr7:146526101-146734852
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	ATF1	chr7:146554072-146554083	K562	blood:	n/a	n/a
2	CCNT2	chr7:146578068-146578178	K562	blood:	n/a	n/a
3	CEBPB	chr7:146653225-146653552	A549	lung:	n/a	chr7:146653389-146653398 chr7:146653389-146653398 chr7:146653387-146653400 chr7:146653389-146653398
4	CEBPB	chr7:146573237-146573380	HepG2	liver:	n/a	chr7:146573302-146573313
5	CEBPB	chr7:146550317-146550587	A549	lung:	n/a	chr7:146550457-146550468 chr7:146550456-146550467
6	CEBPB	chr7:146650625-146650798	K562	blood:	n/a	chr7:146650646-146650655 chr7:146650646-146650655
7	CEBPB	chr7:146645855-146646062	A549	lung:	n/a	n/a
8	CEBPB	chr7:146550344-146550639	HepG2	liver:	n/a	chr7:146550457-146550468 chr7:146550456-146550467
9	CEBPB	chr7:146532369-146532435	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr7:146547720-146547928	HepG2	liver:	n/a	chr7:146547770-146547781
11	CEBPB	chr7:146653286-146653563	HepG2	liver:	n/a	chr7:146653389-146653398 chr7:146653389-146653398 chr7:146653387-146653400 chr7:146653389-146653398
12	CEBPB	chr7:146690455-146690710	HepG2	liver:	n/a	chr7:146690555-146690566
13	CEBPB	chr7:146658691-146659162	ECC-1	luminal epithelium:	n/a	n/a
14	CEBPB	chr7:146631955-146632230	A549	lung:	n/a	n/a
15	CEBPB	chr7:146571872-146572192	A549	lung:	n/a	chr7:146572003-146572012 chr7:146572001-146572014 chr7:146572002-146572013 chr7:146572003-146572012 chr7:146572003-146572012 chr7:146572003-146572012
16	CEBPB	chr7:146571827-146572187	K562	blood:	n/a	chr7:146572003-146572012 chr7:146572001-146572014 chr7:146572002-146572013 chr7:146572003-146572012 chr7:146572003-146572012 chr7:146572003-146572012
17	CEBPB	chr7:146631945-146632234	HepG2	liver:	n/a	n/a
18	CEBPB	chr7:146571842-146572194	H1-hESC	embryonic stem cell:	n/a	chr7:146572003-146572012 chr7:146572001-146572014 chr7:146572002-146572013 chr7:146572003-146572012 chr7:146572003-146572012 chr7:146572003-146572012
19	CEBPB	chr7:146690433-146690694	H1-hESC	embryonic stem cell:	n/a	chr7:146690555-146690566
20	CEBPB	chr7:146571860-146572193	HepG2	liver:	n/a	chr7:146572003-146572012 chr7:146572001-146572014 chr7:146572002-146572013 chr7:146572003-146572012 chr7:146572003-146572012 chr7:146572003-146572012
21	CEBPB	chr7:146690401-146690637	IMR90	lung:	n/a	chr7:146690555-146690566
22	CEBPB	chr7:146650551-146650805	IMR90	lung:	n/a	chr7:146650646-146650655 chr7:146650646-146650655
23	CEBPB	chr7:146702238-146702507	HepG2	liver:	n/a	chr7:146702320-146702331 chr7:146702320-146702333
24	CEBPB	chr7:146673718-146673968	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr7:146547738-146547759	K562	blood:	n/a	n/a
26	CEBPB	chr7:146571852-146572197	IMR90	lung:	n/a	chr7:146572003-146572012 chr7:146572001-146572014 chr7:146572002-146572013 chr7:146572003-146572012 chr7:146572003-146572012 chr7:146572003-146572012
27	CEBPB	chr7:146690528-146690601	K562	blood:	n/a	chr7:146690555-146690566
28	CEBPB	chr7:146582398-146582629	ECC-1	luminal epithelium:	n/a	chr7:146582542-146582553
29	CREB1	chr7:146658679-146659194	ECC-1	luminal epithelium:	n/a	n/a
30	CTCF	chr7:146734040-146734190	HPAF	blood vessel:	n/a	n/a
31	CTCF	chr7:146734040-146734190	HCFaa	heart:	n/a	n/a
32	CTCF	chr7:146658200-146658350	HBMEC	blood vessel:	n/a	chr7:146658320-146658341 chr7:146658325-146658343 chr7:146658279-146658288
33	CTCF	chr7:146658240-146658390	HCPEpiC	choroid plexus:	n/a	chr7:146658320-146658341 chr7:146658325-146658343 chr7:146658279-146658288
34	CTCF	chr7:146658342-146658355	HepG2	liver:	n/a	n/a
35	CTCF	chr7:146658240-146658390	SK-N-SH_RA	brain:	n/a	chr7:146658320-146658341 chr7:146658325-146658343 chr7:146658279-146658288
36	CTCF	chr7:146658200-146658350	MCF-7	breast:	n/a	chr7:146658320-146658341 chr7:146658325-146658343 chr7:146658279-146658288
37	CTCF	chr7:146733716-146733792	GM20000	blood:	n/a	n/a
38	CTCF	chr7:146733960-146734110	HPAF	blood vessel:	n/a	n/a
39	CTCF	chr7:146658720-146658870	HCFaa	heart:	n/a	n/a
40	CTCF	chr7:146658237-146658455	H1-hESC	embryonic stem cell:	n/a	chr7:146658320-146658341 chr7:146658325-146658343 chr7:146658279-146658288
41	CTCF	chr7:146658220-146658370	HPF	lung:	n/a	chr7:146658320-146658341 chr7:146658325-146658343 chr7:146658279-146658288
42	CTCF	chr7:146658272-146658434	ProgFib	skin:	n/a	chr7:146658320-146658341 chr7:146658325-146658343 chr7:146658279-146658288
43	CTCF	chr7:146574364-146574375	GM13977	blood:	n/a	n/a
44	CTCF	chr7:146658220-146658370	HCPEpiC	choroid plexus:	n/a	chr7:146658320-146658341 chr7:146658325-146658343 chr7:146658279-146658288
45	CTCF	chr7:146658240-146658390	HEK293	kidney:	n/a	chr7:146658320-146658341 chr7:146658325-146658343 chr7:146658279-146658288
46	CTCF	chr7:146658290-146658372	MCF-7	breast:	n/a	chr7:146658320-146658341 chr7:146658325-146658343
47	CTCF	chr7:146658220-146658370	Caco-2	colon:	n/a	chr7:146658320-146658341 chr7:146658325-146658343 chr7:146658279-146658288
48	CTCF	chr7:146734047-146734118	Medullo	brain:	n/a	n/a
49	CTCF	chr7:146658283-146658413	MCF-7	breast:	n/a	chr7:146658320-146658341 chr7:146658325-146658343
50	CTCF	chr7:146658260-146658410	WERI-Rb-1	eye:	n/a	chr7:146658320-146658341 chr7:146658325-146658343 chr7:146658279-146658288

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:146635353-146635403	HCF	heart:	n/a
2	chr7:146603166-146603216	MCF10A-Er-Src	breast:	n/a
3	chr7:146635353-146635403	AG09319	gingival:	n/a
4	chr7:146572638-146572688	SK-N-SH	brain:	n/a
5	chr7:146572638-146572688	HIPEpiC	eye:	n/a
6	chr7:146572638-146572688	HRPEpiC	eye:	n/a
7	chr7:146572638-146572688	CMK	blood:	n/a
8	chr7:146603166-146603216	GM12892	blood:	n/a
9	chr7:146572638-146572688	NT2-D1	testis:	n/a
10	chr7:146635353-146635403	LNCaP	prostate:	n/a
11	chr7:146603166-146603216	HMEC	breast:	n/a
12	chr7:146635353-146635403	HRCEpiC	kidney:	n/a
13	chr7:146572638-146572688	Caco-2	colon:	n/a
14	chr7:146572638-146572688	K562	blood:	n/a
15	chr7:146603166-146603216	PFSK-1	brain:	n/a
16	chr7:146635353-146635403	NH-A	brain:	n/a
17	chr7:146635353-146635403	H1-hESC	embryonic stem cell:	embryo
18	chr7:146603166-146603216	HIPEpiC	eye:	n/a
19	chr7:146603166-146603216	Hepatocyte	liver:	n/a
20	chr7:146603166-146603216	GM19239	blood:	n/a
21	chr7:146635353-146635403	SKMC	muscle:	n/a
22	chr7:146635353-146635403	Jurkat	blood:	n/a
23	chr7:146572638-146572688	HepG2	liver:	n/a
24	chr7:146572638-146572688	SAEC	small airway:	n/a
25	chr7:146603166-146603216	AG09319	gingival:	n/a
26	chr7:146603166-146603216	HCF	heart:	n/a
27	chr7:146572638-146572688	NHDF-neo	bronchial:	n/a
28	chr7:146572638-146572688	Hela-S3	cervix:	n/a
29	chr7:146635353-146635403	A549	lung:	n/a
30	chr7:146603166-146603216	HEK293	kidney:	embryo
31	chr7:146603166-146603216	SKMC	muscle:	n/a
32	chr7:146635353-146635403	NHBE	bronchial:	n/a
33	chr7:146572638-146572688	PFSK-1	brain:	n/a
34	chr7:146635353-146635403	AG09309	skin:	n/a
35	chr7:146603166-146603216	Jurkat	blood:	n/a
36	chr7:146603166-146603216	SK-N-MC	brain:	n/a
37	chr7:146603166-146603216	AG10803	skin:	n/a
38	chr7:146603166-146603216	BE2_C	brain:	n/a
39	chr7:146635353-146635403	AoSMC	blood vessel:	n/a
40	chr7:146603166-146603216	LNCaP	prostate:	n/a
41	chr7:146635353-146635403	HepG2	liver:	n/a
42	chr7:146603166-146603216	HAEpiC	amniotic membrane:	n/a
43	chr7:146572638-146572688	NHBE	bronchial:	n/a
44	chr7:146635353-146635403	HUVEC	blood vessel:	n/a
45	chr7:146572638-146572688	RPTEC	kidney:	n/a
46	chr7:146603166-146603216	Hela-S3	cervix:	n/a
47	chr7:146572638-146572688	GM12892	blood:	n/a
48	chr7:146635353-146635403	HEK293	kidney:	embryo
49	chr7:146635353-146635403	SK-N-MC	brain:	n/a
50	chr7:146603166-146603216	IMR90	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr7:146657758..146660161-chr7:146662601..146665251,2	K562	blood:
2	chr7:146715781..146717659-chr7:146720196..146724156,3	K562	blood:
3	chr7:146531380..146533231-chr7:146533268..146535989,2	K562	blood:
4	chr11:86510283..86512929-chr7:146532947..146535829,2	MCF-7	breast:
5	chr7:146651547..146653225-chr7:146656495..146658548,2	K562	blood:
6	chr7:146728137..146729642-chr7:146730753..146732443,2	K562	blood:
7	chr7:146728137..146729642-chr7:146730753..146732443,2	K562	blood:
8	chr7:146570862..146573024-chr7:146579800..146582486,2	K562	blood:
9	chr7:146651547..146653225-chr7:146656495..146658548,2	K562	blood:
10	chr7:146715781..146717659-chr7:146720196..146724156,3	K562	blood:
11	chr7:146500988..146503359-chr7:146527735..146530660,2	K562	blood:
12	chr7:146537182..146538796-chr7:146543002..146544884,2	K562	blood:
13	chr7:146570862..146573024-chr7:146579800..146582486,2	K562	blood:
14	chr7:146531380..146533231-chr7:146533268..146535989,2	K562	blood:
15	chr7:146537182..146538796-chr7:146543002..146544884,2	K562	blood:
16	chr7:146657758..146660161-chr7:146662601..146665251,2	K562	blood:

Variant related genes	Relation type
ENSG00000221766	TF binding region
ENSG00000221766	CpG island
ENSG00000150687	chromatin interactions

Extended variants
information (count: 2665 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:2665 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs73459343	chr7:146526204-146526205	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs542877811	chr7:146526212-146526213	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs190684560	chr7:146526295-146526296	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs573219035	chr7:146526300-146526301	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs545271184	chr7:146526346-146526347	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs563744378	chr7:146526370-146526371	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs532728592	chr7:146526392-146526393	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs115096548	chr7:146526417-146526418	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs71525975	chr7:146526425-146526426	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs563287540	chr7:146526435-146526436	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs149335116	chr7:146526441-146526442	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs548920755	chr7:146526563-146526564	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs182914917	chr7:146526594-146526595	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs528396977	chr7:146526597-146526598	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs79856572	chr7:146526650-146526651	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs539238208	chr7:146526657-146526658	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs377615396	chr7:146526658-146526659	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs571554873	chr7:146526701-146526702	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs554246012	chr7:146526780-146526781	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs551911779	chr7:146529241-146529242	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs142415181	chr7:146529309-146529310	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs369853592	chr7:146529342-146529343	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs556040401	chr7:146529357-146529358	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs369157244	chr7:146529488-146529489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs563025560	chr7:146529526-146529527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs187219941	chr7:146529547-146529548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs190953075	chr7:146529558-146529559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs548777413	chr7:146529562-146529563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs200037272	chr7:146529595-146529596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs562110360	chr7:146529615-146529616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs28648535	chr7:146529693-146529694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs527992525	chr7:146529709-146529710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs144665811	chr7:146529711-146529712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs571155662	chr7:146529716-146529717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs577526039	chr7:146529762-146529763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs529130551	chr7:146529763-146529764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs568942806	chr7:146529764-146529765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs551868585	chr7:146529771-146529772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs371934317	chr7:146529772-146529773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs111974923	chr7:146529773-146529774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs533896710	chr7:146529791-146529792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs534458194	chr7:146529810-146529811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs185971209	chr7:146529879-146529880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs190038861	chr7:146529928-146529929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs138552391	chr7:146529929-146529930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs141139617	chr7:146529936-146529937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs553696019	chr7:146529937-146529938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs572133263	chr7:146529944-146529945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs546210574	chr7:146529962-146529963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs75814474	chr7:146530023-146530024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Glioblastoma multiforme	18628472	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	16272173	CNVD
Myxofibrosarcoma	16751306	CNVD
Stuttering	21108403	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17133270	CNVD
Schizophrenia	17646849	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Lung adenocarcinoma	17086460	CNVD
Gastric adenocarcinoma	19115996	CNVD
Pancreatitis	21956041	CNVD
Acute myeloid leukemia	16864856	CNVD
Gastric cancer	16891809	CNVD
Lung cancer	17086460	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20808228	CNVD
Schizophrenia	20838587	CNVD
Schizophrenia	20718829	CNVD
Neuropsychiatric disorder	21827697	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21509527	CNVD
Autism	20964600	CNVD
Epilepsy	17646849	CNVD
Mental retardation	19896112	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Glioma	20126413	CNVD
Bipolar disorder	19114987	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:153 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:146526200-146526800	Enhancers	Pancreatic Islets	Pancreatic Islet
2	chr7:146529200-146529400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr7:146529400-146537800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr7:146536800-146537000	Bivalent/Poised TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr7:146546400-146547200	Enhancers	Brain Germinal Matrix	brain
6	chr7:146557400-146557600	Enhancers	Brain Germinal Matrix	brain
7	chr7:146557600-146558200	Weak transcription	Brain Germinal Matrix	brain
8	chr7:146558200-146558400	Enhancers	Brain Germinal Matrix	brain
9	chr7:146558400-146559600	Weak transcription	Brain Germinal Matrix	brain
10	chr7:146558800-146560200	Enhancers	Fetal Brain Male	brain
11	chr7:146559000-146560200	Enhancers	Fetal Brain Female	brain
12	chr7:146559400-146559600	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr7:146559400-146559800	Enhancers	Cortex derived primary cultured neurospheres	brain
14	chr7:146559600-146560600	Enhancers	Brain Germinal Matrix	brain
15	chr7:146561400-146561800	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr7:146561400-146561800	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr7:146561800-146562800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr7:146562800-146563000	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr7:146571800-146573200	Enhancers	Fetal Brain Male	brain
20	chr7:146571800-146573800	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr7:146572000-146572800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr7:146572000-146572800	Enhancers	Brain Germinal Matrix	brain
23	chr7:146572000-146573400	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr7:146572000-146573400	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr7:146572000-146574000	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr7:146572000-146574200	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr7:146572200-146572800	Enhancers	Cortex derived primary cultured neurospheres	brain
28	chr7:146572200-146573400	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr7:146572200-146573600	Enhancers	Fetal Brain Female	brain
30	chr7:146572400-146573400	Enhancers	Fetal Stomach	stomach
31	chr7:146572600-146573400	Enhancers	H1 Cell Line	embryonic stem cell
32	chr7:146572600-146573400	Enhancers	H9 Cell Line	embryonic stem cell
33	chr7:146572600-146573600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr7:146572800-146573200	Enhancers	Ovary	ovary
35	chr7:146572800-146574000	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr7:146573200-146573800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr7:146573200-146574000	Enhancers	Fetal Lung	lung
38	chr7:146573800-146577200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
39	chr7:146577200-146577600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
40	chr7:146577600-146578200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr7:146582800-146584400	Enhancers	Fetal Brain Male	brain
42	chr7:146587000-146587600	Enhancers	Pancreatic Islets	Pancreatic Islet
43	chr7:146589000-146589400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr7:146589200-146589600	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr7:146589400-146589800	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr7:146602200-146602800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
47	chr7:146602600-146602800	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
48	chr7:146602800-146603000	Active TSS	ES-I3 Cell Line	embryonic stem cell
49	chr7:146614000-146615400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr7:146616400-146617400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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