Variant report

Variant	nsv1034620
Chromosome Location	chr7:84701267-84791576
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	ATF2	chr7:84789526-84789901	GM12878	blood:	n/a	n/a
2	BATF	chr7:84789624-84789929	GM12878	blood:	n/a	chr7:84789692-84789702
3	BATF	chr7:84789567-84789977	GM12878	blood:	n/a	chr7:84789692-84789702
4	BCL11A	chr7:84789578-84789942	GM12878	blood:	n/a	n/a
5	BCL11A	chr7:84789728-84789890	GM12878	blood:	n/a	n/a
6	BHLHE40	chr7:84789641-84789872	GM12878	blood:	n/a	n/a
7	CBX3	chr7:84743653-84744093	HCT-116	colon:	n/a	n/a
8	CEBPB	chr7:84733601-84734254	HCT-116	colon:	n/a	chr7:84733766-84733779
9	CEBPB	chr7:84742249-84742569	IMR90	lung:	n/a	chr7:84742423-84742434 chr7:84742425-84742434 chr7:84742321-84742333 chr7:84742425-84742434 chr7:84742425-84742434 chr7:84742424-84742435 chr7:84742425-84742434 chr7:84742423-84742436
10	CEBPB	chr7:84742269-84742596	HepG2	liver:	n/a	chr7:84742423-84742434 chr7:84742425-84742434 chr7:84742321-84742333 chr7:84742425-84742434 chr7:84742425-84742434 chr7:84742424-84742435 chr7:84742425-84742434 chr7:84742423-84742436
11	CEBPB	chr7:84716033-84716591	HepG2	liver:	n/a	chr7:84716195-84716206 chr7:84716195-84716208
12	CEBPB	chr7:84716026-84716363	IMR90	lung:	n/a	chr7:84716195-84716206 chr7:84716195-84716208
13	CEBPB	chr7:84700492-84701473	IMR90	lung:	n/a	n/a
14	CEBPB	chr7:84716021-84716380	A549	lung:	n/a	chr7:84716195-84716206 chr7:84716195-84716208
15	CEBPB	chr7:84733770-84734122	IMR90	lung:	n/a	n/a
16	CEBPB	chr7:84732633-84732996	Hela-S3	cervix:	n/a	chr7:84732645-84732656 chr7:84732645-84732656 chr7:84732644-84732661
17	CEBPB	chr7:84733365-84734152	Hela-S3	cervix:	n/a	chr7:84733766-84733779
18	CEBPB	chr7:84722951-84723231	IMR90	lung:	n/a	chr7:84723072-84723083
19	CEBPB	chr7:84749286-84749604	Hela-S3	cervix:	n/a	chr7:84749442-84749453 chr7:84749440-84749453 chr7:84749440-84749451
20	CEBPB	chr7:84789515-84789806	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr7:84749305-84749558	K562	blood:	n/a	chr7:84749442-84749453 chr7:84749440-84749453 chr7:84749440-84749451
22	CEBPB	chr7:84765248-84765846	Hela-S3	cervix:	n/a	chr7:84765742-84765754
23	CEBPB	chr7:84716035-84716343	H1-hESC	embryonic stem cell:	n/a	chr7:84716195-84716206 chr7:84716195-84716208
24	CEBPB	chr7:84746244-84746431	HepG2	liver:	n/a	chr7:84746369-84746380
25	CEBPB	chr7:84742392-84742488	K562	blood:	n/a	chr7:84742423-84742434 chr7:84742425-84742434 chr7:84742425-84742434 chr7:84742425-84742434 chr7:84742424-84742435 chr7:84742425-84742434 chr7:84742423-84742436
26	CEBPB	chr7:84779040-84779246	IMR90	lung:	n/a	n/a
27	CEBPB	chr7:84749259-84749629	IMR90	lung:	n/a	chr7:84749442-84749453 chr7:84749440-84749453 chr7:84749440-84749451
28	CEBPB	chr7:84749355-84749592	H1-hESC	embryonic stem cell:	n/a	chr7:84749442-84749453 chr7:84749440-84749453 chr7:84749440-84749451
29	CEBPB	chr7:84733780-84734161	HCT-116	colon:	n/a	n/a
30	CEBPB	chr7:84772657-84772840	HepG2	liver:	n/a	chr7:84772671-84772682
31	CEBPB	chr7:84789472-84789832	IMR90	lung:	n/a	n/a
32	CEBPB	chr7:84749286-84749595	A549	lung:	n/a	chr7:84749442-84749453 chr7:84749440-84749453 chr7:84749440-84749451
33	CEBPB	chr7:84742490-84742511	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr7:84722987-84723198	HepG2	liver:	n/a	chr7:84723072-84723083
35	CEBPB	chr7:84742261-84742529	A549	lung:	n/a	chr7:84742423-84742434 chr7:84742425-84742434 chr7:84742321-84742333 chr7:84742425-84742434 chr7:84742425-84742434 chr7:84742424-84742435 chr7:84742425-84742434 chr7:84742423-84742436
36	CEBPB	chr7:84749271-84749633	HepG2	liver:	n/a	chr7:84749442-84749453 chr7:84749440-84749453 chr7:84749440-84749451
37	CHD2	chr7:84789700-84789873	GM12878	blood:	n/a	n/a
38	CTCF	chr7:84754520-84754670	HepG2	liver:	n/a	n/a
39	CTCF	chr7:84754540-84754690	BE2_C	brain:	n/a	n/a
40	CTCF	chr7:84754540-84754690	SK-N-SH_RA	brain:	n/a	n/a
41	E2F4	chr7:84761356-84761581	MCF10A-Er-Src	breast:	n/a	n/a
42	E2F4	chr7:84767326-84767350	MCF10A-Er-Src	breast:	n/a	n/a
43	E2F4	chr7:84768413-84768565	MCF10A-Er-Src	breast:	n/a	n/a
44	E2F4	chr7:84781642-84781778	MCF10A-Er-Src	breast:	n/a	n/a
45	E2F4	chr7:84706573-84706762	MCF10A-Er-Src	breast:	n/a	n/a
46	E2F4	chr7:84766523-84766756	MCF10A-Er-Src	breast:	n/a	n/a
47	E2F4	chr7:84752385-84752559	MCF10A-Er-Src	breast:	n/a	n/a
48	E2F4	chr7:84727289-84727489	MCF10A-Er-Src	breast:	n/a	n/a
49	EBF1	chr7:84789728-84789928	GM12878	blood:	n/a	n/a
50	ELF1	chr7:84765137-84765872	SK-N-SH	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:84783791-84783841	T-47D	breast:	n/a
2	chr7:84783791-84783841	HIPEpiC	eye:	n/a
3	chr7:84789871-84789921	BJ	skin:	n/a
4	chr7:84789871-84789921	Caco-2	colon:	n/a
5	chr7:84783791-84783841	LNCaP	prostate:	n/a
6	chr7:84783791-84783841	AG10803	skin:	n/a
7	chr7:84789871-84789921	U87	brain:	n/a
8	chr7:84789871-84789921	HIPEpiC	eye:	n/a
9	chr7:84789871-84789921	GM12891	blood:	n/a
10	chr7:84783791-84783841	NH-A	brain:	n/a
11	chr7:84789871-84789921	NHDF-neo	bronchial:	n/a
12	chr7:84783791-84783841	Hela-S3	cervix:	n/a
13	chr7:84783791-84783841	GM06990	blood:	n/a
14	chr7:84783791-84783841	NT2-D1	testis:	n/a
15	chr7:84789871-84789921	HRPEpiC	eye:	n/a
16	chr7:84783791-84783841	Caco-2	colon:	n/a
17	chr7:84789871-84789921	GM12892	blood:	n/a
18	chr7:84789871-84789921	A549	lung:	n/a
19	chr7:84789871-84789921	HCF	heart:	n/a
20	chr7:84783791-84783841	HL-60	blood:	n/a
21	chr7:84783791-84783841	AG04450	lung:	fetal
22	chr7:84783791-84783841	HMEC	breast:	n/a
23	chr7:84789871-84789921	AoSMC	blood vessel:	n/a
24	chr7:84783791-84783841	PFSK-1	brain:	n/a
25	chr7:84783791-84783841	AG04449	skin:	fetal
26	chr7:84789871-84789921	K562	blood:	n/a
27	chr7:84789871-84789921	HPAEpiC	pulmonary alveolar:	n/a
28	chr7:84789871-84789921	H1-hESC	embryonic stem cell:	embryo
29	chr7:84789871-84789921	AG09309	skin:	n/a
30	chr7:84783791-84783841	HNPCEpiC	eye:	n/a
31	chr7:84783791-84783841	Jurkat	blood:	n/a
32	chr7:84783791-84783841	HCF	heart:	n/a
33	chr7:84783791-84783841	MCF-7	breast:	n/a
34	chr7:84783791-84783841	H1-hESC	embryonic stem cell:	embryo
35	chr7:84783791-84783841	AoSMC	blood vessel:	n/a
36	chr7:84789871-84789921	CMK	blood:	n/a
37	chr7:84789871-84789921	HRCEpiC	kidney:	n/a
38	chr7:84783791-84783841	PANC-1	pancreas:	n/a
39	chr7:84783791-84783841	SKMC	muscle:	n/a
40	chr7:84783791-84783841	HepG2	liver:	n/a
41	chr7:84783791-84783841	HPAEpiC	pulmonary alveolar:	n/a
42	chr7:84789871-84789921	T-47D	breast:	n/a
43	chr7:84789871-84789921	AG04450	lung:	fetal
44	chr7:84789871-84789921	SK-N-SH	brain:	n/a
45	chr7:84783791-84783841	BJ	skin:	n/a
46	chr7:84789871-84789921	MCF-7	breast:	n/a
47	chr7:84783791-84783841	NB4	blood:	n/a
48	chr7:84783791-84783841	ECC-1	luminal epithelium:	n/a
49	chr7:84783791-84783841	BE2_C	brain:	n/a
50	chr7:84783791-84783841	GM12891	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:84710975..84713239-chr7:84714640..84716583,2	K562	blood:
2	chr7:84710975..84713239-chr7:84714640..84716583,2	K562	blood:
3	chr7:84670637..84671142-chr7:84753974..84754698,2	MCF-7	breast:
4	chr7:84752077..84754920-chr7:84758473..84761115,2	K562	blood:
5	chr7:84734863..84737754-chr7:84754165..84755830,2	MCF-7	breast:
6	chr20:52464253..52464773-chr7:84783688..84784207,2	MCF-7	breast:
7	chr7:84783479..84785634-chr7:84790820..84792912,2	K562	blood:
8	chr7:84717702..84719769-chr7:84720076..84722909,2	K562	blood:
9	chr7:84718632..84720833-chr7:84723046..84725256,2	K562	blood:
10	chr7:84752077..84754920-chr7:84758473..84761115,2	K562	blood:
11	chr3:4928813..4929334-chr7:84742209..84742729,2	MCF-7	breast:
12	chr7:84783738..84785912-chr7:84791930..84794783,2	K562	blood:
13	chr7:84717702..84719769-chr7:84720076..84722909,2	K562	blood:
14	chr7:84718632..84720833-chr7:84723046..84725256,2	K562	blood:
15	chr7:84734863..84737754-chr7:84754165..84755830,2	MCF-7	breast:
16	chr7:84783479..84785634-chr7:84790820..84792912,2	K562	blood:

Variant related genes	Relation type
SEMA3D	TF binding region
SEMA3D	CpG island
ENSG00000235978	chromatin interactions

Extended variants
information (count: 3134 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:3134 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185467597	chr7:84701271-84701272	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs575897682	chr7:84701288-84701289	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs543021695	chr7:84701361-84701362	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs189881623	chr7:84701371-84701372	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs573618114	chr7:84701417-84701418	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs140146139	chr7:84701461-84701462	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs559156418	chr7:84701473-84701474	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs578041549	chr7:84701534-84701535	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs545218921	chr7:84701559-84701560	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs554290206	chr7:84701600-84701601	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs182158407	chr7:84701641-84701642	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs149916817	chr7:84701644-84701645	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs113531483	chr7:84701661-84701662	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs188898529	chr7:84701750-84701751	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs528824670	chr7:84701754-84701755	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs547201980	chr7:84701773-84701774	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs571791549	chr7:84701785-84701786	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs145809090	chr7:84701818-84701819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs551146986	chr7:84701844-84701845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs569746816	chr7:84701868-84701869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs536620043	chr7:84701893-84701894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs554969181	chr7:84701898-84701899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs139338794	chr7:84701932-84701933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs373966679	chr7:84701953-84701954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs573581833	chr7:84702016-84702017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs534640710	chr7:84702030-84702031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs553128924	chr7:84702125-84702126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs148990277	chr7:84702141-84702142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs6957484	chr7:84702152-84702153	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs563598620	chr7:84702171-84702172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs575831914	chr7:84702190-84702191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs543023316	chr7:84702192-84702193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs114634487	chr7:84702273-84702274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs369263940	chr7:84702306-84702307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs147788437	chr7:84702314-84702315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs201838826	chr7:84702317-84702318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs547265159	chr7:84702318-84702319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs193226372	chr7:84702355-84702356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs371924373	chr7:84702373-84702374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs532633114	chr7:84702385-84702386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs375641656	chr7:84702414-84702415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs78169787	chr7:84702429-84702430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs569673740	chr7:84702439-84702440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs552152950	chr7:84702508-84702509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs536715128	chr7:84702516-84702517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs548579689	chr7:84702526-84702527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs566875929	chr7:84702553-84702554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs147108788	chr7:84702569-84702570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs553031923	chr7:84702586-84702587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs138523348	chr7:84702610-84702611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
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
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Biliary cancer	19435499	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	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
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Neurodevelopmental disorder	22521361	CNVD
Metanephric adenoma	20802469	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Williams-beuren syndrome	16826523	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	19318497	CNVD
Multiple myeloma	16616336	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Schizophrenia	17879154	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Autism	20858243	CNVD
Renal cell carcinoma	18194544	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21611746	CNVD

Chromatin state (count:304 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:84693000-84705400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr7:84696000-84717600	Weak transcription	Fetal Stomach	stomach
3	chr7:84698400-84704800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr7:84699400-84701400	Enhancers	Fetal Kidney	kidney
5	chr7:84699800-84703000	Weak transcription	HUVEC	blood vessel
6	chr7:84700000-84701400	Enhancers	NHEK	skin
7	chr7:84700000-84704400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr7:84700600-84701400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
9	chr7:84700600-84701800	Strong transcription	Fetal Lung	lung
10	chr7:84700600-84705000	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr7:84700800-84704000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr7:84701200-84701600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr7:84701200-84715400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr7:84701400-84704800	Weak transcription	Fetal Kidney	kidney
15	chr7:84701400-84709800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr7:84701800-84707200	Weak transcription	Fetal Lung	lung
17	chr7:84703400-84703800	Enhancers	Muscle Satellite Cultured Cells	--
18	chr7:84704000-84704400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr7:84704000-84705600	Enhancers	Fetal Intestine Large	intestine
20	chr7:84704400-84704800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr7:84704800-84705200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr7:84704800-84705200	Enhancers	Fetal Kidney	kidney
23	chr7:84704800-84705400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr7:84705000-84705600	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr7:84705000-84705600	Enhancers	Stomach Mucosa	stomach
26	chr7:84705200-84705400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr7:84705200-84707000	Weak transcription	Fetal Kidney	kidney
28	chr7:84705400-84705600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr7:84705400-84706200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr7:84707000-84707200	Enhancers	Fetal Kidney	kidney
31	chr7:84707200-84707600	Weak transcription	Fetal Kidney	kidney
32	chr7:84707200-84707800	Enhancers	Fetal Lung	lung
33	chr7:84707400-84707600	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr7:84707600-84707800	Enhancers	Fetal Kidney	kidney
35	chr7:84707600-84708000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr7:84707600-84708200	Flanking Bivalent TSS/Enh	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr7:84707800-84710800	Weak transcription	Fetal Lung	lung
38	chr7:84707800-84711000	Weak transcription	Fetal Kidney	kidney
39	chr7:84708200-84708600	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr7:84709800-84710400	Enhancers	Breast Myoepithelial Primary Cells	Breast
41	chr7:84710400-84710800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
42	chr7:84710800-84711000	Enhancers	Breast Myoepithelial Primary Cells	Breast
43	chr7:84710800-84711600	Enhancers	Fetal Heart	heart
44	chr7:84710800-84711600	Enhancers	Fetal Lung	lung
45	chr7:84711000-84711600	Enhancers	Fetal Kidney	kidney
46	chr7:84711000-84719600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
47	chr7:84711600-84719400	Weak transcription	Fetal Lung	lung
48	chr7:84717600-84719600	Enhancers	Fetal Stomach	stomach
49	chr7:84719200-84719800	Enhancers	Duodenum Smooth Muscle	Duodenum
50	chr7:84719200-84721400	Enhancers	Rectal Smooth Muscle	rectum

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