Variant report

Variant	esv1825159
Chromosome Location	chr7:118640865-118842361
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:732)
CpG islands
(count:61)
Chromatin interactive
region (count:37)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr7:118650678-118650912	GM12878	blood:	n/a	n/a
2	BHLHE40	chr7:118838082-118838260	GM12878	blood:	n/a	n/a
3	BHLHE40	chr7:118816087-118816420	GM12878	blood:	n/a	n/a
4	BRCA1	chr7:118747696-118747725	GM12878	blood:	n/a	n/a
5	CBX3	chr7:118807512-118807928	HCT-116	colon:	n/a	n/a
6	CCNT2	chr7:118787886-118788025	K562	blood:	n/a	n/a
7	CEBPB	chr7:118713529-118713772	A549	lung:	n/a	chr7:118713628-118713641 chr7:118713591-118713604 chr7:118713668-118713679 chr7:118713628-118713639 chr7:118713630-118713641 chr7:118713591-118713603 chr7:118713668-118713681 chr7:118713628-118713641
8	CEBPB	chr7:118766145-118766405	HepG2	liver:	n/a	n/a
9	CEBPB	chr7:118686542-118686614	A549	lung:	n/a	n/a
10	CEBPB	chr7:118730966-118731278	Hela-S3	cervix:	n/a	chr7:118731238-118731251
11	CEBPB	chr7:118664287-118664601	A549	lung:	n/a	n/a
12	CEBPB	chr7:118646259-118646292	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr7:118742647-118742847	HepG2	liver:	n/a	chr7:118742808-118742821 chr7:118742809-118742820 chr7:118742808-118742821
14	CEBPB	chr7:118713490-118713806	HepG2	liver:	n/a	chr7:118713628-118713641 chr7:118713591-118713604 chr7:118713668-118713679 chr7:118713628-118713639 chr7:118713630-118713641 chr7:118713591-118713603 chr7:118713668-118713681 chr7:118713628-118713641
15	CEBPB	chr7:118640929-118641155	A549	lung:	n/a	chr7:118641131-118641144
16	CEBPB	chr7:118840953-118841173	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr7:118640833-118641182	HepG2	liver:	n/a	chr7:118641131-118641144
18	CEBPB	chr7:118742621-118742863	A549	lung:	n/a	chr7:118742808-118742821 chr7:118742809-118742820 chr7:118742808-118742821
19	CEBPB	chr7:118706103-118706303	A549	lung:	n/a	n/a
20	CHD2	chr7:118816031-118816309	H1-hESC	embryonic stem cell:	n/a	n/a
21	CREB1	chr7:118815972-118816285	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr7:118838080-118838230	HEK293	kidney:	n/a	n/a
23	CTCF	chr7:118788380-118788530	HCT-116	colon:	n/a	n/a
24	CTCF	chr7:118838016-118838315	K562	blood:	n/a	n/a
25	CTCF	chr7:118816120-118816270	GM12878	blood:	n/a	n/a
26	CTCF	chr7:118816027-118816384	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr7:118816128-118816390	K562	blood:	n/a	n/a
28	CTCF	chr7:118838120-118838270	HRPEpiC	eye:	n/a	n/a
29	CTCF	chr7:118805496-118805529	MCF-7	breast:	n/a	n/a
30	CTCF	chr7:118816075-118816440	SK-N-SH_RA	brain:	n/a	n/a
31	CTCF	chr7:118838120-118838270	BJ	skin:	n/a	n/a
32	CTCF	chr7:118816180-118816330	GM12874	blood:	n/a	n/a
33	CTCF	chr7:118816103-118816382	MCF-7	breast:	n/a	n/a
34	CTCF	chr7:118816180-118816330	WERI-Rb-1	eye:	n/a	n/a
35	CTCF	chr7:118838100-118838250	HEK293	kidney:	n/a	n/a
36	CTCF	chr7:118837922-118837961	GM12891	blood:	n/a	n/a
37	CTCF	chr7:118727500-118727650	WERI-Rb-1	eye:	n/a	n/a
38	CTCF	chr7:118816160-118816310	HEK293	kidney:	n/a	n/a
39	CTCF	chr7:118838021-118838312	HepG2	liver:	n/a	n/a
40	CTCF	chr7:118816160-118816310	NHEK	skin:	n/a	n/a
41	CTCF	chr7:118838060-118838210	GM12870	blood:	n/a	n/a
42	CTCF	chr7:118816140-118816290	K562	blood:	n/a	n/a
43	CTCF	chr7:118837996-118838239	T-47D	breast:	n/a	n/a
44	CTCF	chr7:118816300-118816450	WI-38	lung:	n/a	n/a
45	CTCF	chr7:118838080-118838230	GM06990	blood:	n/a	n/a
46	CTCF	chr7:118838080-118838230	GM12869	blood:	n/a	n/a
47	CTCF	chr7:118838120-118838270	GM12874	blood:	n/a	n/a
48	CTCF	chr7:118837640-118837790	GM12869	blood:	n/a	n/a
49	CTCF	chr7:118838089-118838235	ECC-1	luminal epithelium:	n/a	n/a
50	CTCF	chr7:118838100-118838250	GM12865	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:118741415-118741465	NH-A	brain:	n/a
2	chr7:118741415-118741465	NHBE	bronchial:	n/a
3	chr7:118741415-118741465	BE2_C	brain:	n/a
4	chr7:118741415-118741465	HCM	heart:	n/a
5	chr7:118741415-118741465	PFSK-1	brain:	n/a
6	chr7:118741415-118741465	U87	brain:	n/a
7	chr7:118741415-118741465	NB4	blood:	n/a
8	chr7:118741415-118741465	T-47D	breast:	n/a
9	chr7:118741415-118741465	Caco-2	colon:	n/a
10	chr7:118741415-118741465	A549	lung:	n/a
11	chr7:118741415-118741465	AG09319	gingival:	n/a
12	chr7:118741415-118741465	Hela-S3	cervix:	n/a
13	chr7:118741415-118741465	SKMC	muscle:	n/a
14	chr7:118741415-118741465	HIPEpiC	eye:	n/a
15	chr7:118741415-118741465	HepG2	liver:	n/a
16	chr7:118741415-118741465	MCF10A-Er-Src	breast:	n/a
17	chr7:118741415-118741465	GM12892	blood:	n/a
18	chr7:118741415-118741465	AG10803	skin:	n/a
19	chr7:118741415-118741465	SK-N-MC	brain:	n/a
20	chr7:118741415-118741465	SK-N-SH_RA	brain:	n/a
21	chr7:118741415-118741465	HCPEpiC	choroid plexus:	n/a
22	chr7:118741415-118741465	ProgFib	skin:	n/a
23	chr7:118741415-118741465	Hepatocyte	liver:	n/a
24	chr7:118741415-118741465	HEK293	kidney:	embryo
25	chr7:118741415-118741465	AoSMC	blood vessel:	n/a
26	chr7:118741415-118741465	MCF-7	breast:	n/a
27	chr7:118741415-118741465	AG09309	skin:	n/a
28	chr7:118741415-118741465	AG04449	skin:	fetal
29	chr7:118741415-118741465	SK-N-SH	brain:	n/a
30	chr7:118741415-118741465	AG04450	lung:	fetal
31	chr7:118741415-118741465	K562	blood:	n/a
32	chr7:118741415-118741465	GM19239	blood:	n/a
33	chr7:118741415-118741465	H1-hESC	embryonic stem cell:	embryo
34	chr7:118741415-118741465	HL-60	blood:	n/a
35	chr7:118741415-118741465	NT2-D1	testis:	n/a
36	chr7:118741415-118741465	HEEpiC	esophagus:	n/a
37	chr7:118741415-118741465	LNCaP	prostate:	n/a
38	chr7:118741415-118741465	SAEC	small airway:	n/a
39	chr7:118741415-118741465	HCF	heart:	n/a
40	chr7:118741415-118741465	HCT-116	colon:	n/a
41	chr7:118741415-118741465	PANC-1	pancreas:	n/a
42	chr7:118741415-118741465	Jurkat	blood:	n/a
43	chr7:118741415-118741465	CMK	blood:	n/a
44	chr7:118741415-118741465	BJ	skin:	n/a
45	chr7:118741415-118741465	ECC-1	luminal epithelium:	n/a
46	chr7:118741415-118741465	HPAEpiC	pulmonary alveolar:	n/a
47	chr7:118741415-118741465	HNPCEpiC	eye:	n/a
48	chr7:118741415-118741465	GM12878	blood:	n/a
49	chr7:118741415-118741465	HUVEC	blood vessel:	n/a
50	chr7:118741415-118741465	IMR90	lung:	fetal

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:118686305..118688542-chr7:118689075..118691425,2	MCF-7	breast:
2	chr7:118558340..118559254-chr7:118837696..118838683,4	MCF-7	breast:
3	chr7:118782215..118784443-chr7:118786067..118788168,2	K562	blood:
4	chr7:118637455..118639784-chr7:118654717..118656624,2	K562	blood:
5	chr7:118654140..118657090-chr7:118659038..118660634,2	K562	blood:
6	chr7:117992682..117993833-chr7:118815599..118816513,3	MCF-7	breast:
7	chr7:118646033..118648474-chr7:118650936..118653090,2	K562	blood:
8	chr7:118829678..118832309-chr7:118833350..118835537,2	MCF-7	breast:
9	chr7:118654140..118657090-chr7:118659038..118660634,2	K562	blood:
10	chr7:118829678..118832309-chr7:118833350..118835537,2	MCF-7	breast:
11	chr7:118637455..118640247-chr7:118654338..118656624,3	K562	blood:
12	chr7:118635764..118637617-chr7:118641365..118644121,2	MCF-7	breast:
13	chr7:117992579..117993168-chr7:118815740..118816656,2	K562	blood:
14	chr7:118686305..118688542-chr7:118689075..118691425,2	MCF-7	breast:
15	chr7:118558392..118559287-chr7:118815693..118816489,5	MCF-7	breast:
16	chr7:118800323..118802977-chr7:118807126..118809160,2	K562	blood:
17	chr7:118611978..118614798-chr7:118654699..118657373,2	K562	blood:
18	chr7:118823416..118825410-chr7:118825629..118827229,2	K562	blood:
19	chr7:118742557..118744399-chr7:118756096..118757786,2	K562	blood:
20	chr7:118646033..118648474-chr7:118650936..118653090,2	K562	blood:
21	chr7:118733515..118736474-chr7:118742172..118744304,2	K562	blood:
22	chr7:118629006..118631002-chr7:118732998..118734533,2	K562	blood:
23	chr7:118742557..118744399-chr7:118756096..118757786,2	K562	blood:
24	chr7:118510382..118510908-chr7:118815972..118816682,2	MCF-7	breast:
25	chr7:118658923..118660731-chr7:118674082..118677043,2	K562	blood:
26	chr7:118558904..118559746-chr7:118816086..118816731,2	MCF-7	breast:
27	chr7:118683308..118685172-chr7:118689159..118691068,2	K562	blood:
28	chr7:117992651..117993374-chr7:118815864..118816654,2	MCF-7	breast:
29	chr7:118800323..118802977-chr7:118807126..118809160,2	K562	blood:
30	chr7:118733515..118736474-chr7:118742172..118744304,2	K562	blood:
31	chr7:118823416..118825410-chr7:118825629..118827229,2	K562	blood:
32	chr7:118658923..118660731-chr7:118674082..118677043,2	K562	blood:
33	chr7:117390803..117391431-chr7:118815895..118816706,2	MCF-7	breast:
34	chr7:118782215..118784443-chr7:118786067..118788168,2	K562	blood:
35	chr7:118288299..118289194-chr7:118816171..118816706,2	MCF-7	breast:
36	chr7:118683308..118685172-chr7:118689159..118691068,2	K562	blood:
37	chr7:118792620..118793489-chr9:140473359..140473903,2	Hela-S3	cervix:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CTTNBP2-7	chr7:118818231-118819203	NONHSAT122980

No data

Variant related genes	Relation type
ENSG00000270516	TF binding region
ENSG00000270516	CpG island
ENSG00000148399	chromatin interactions

Extended variants
information (count: 3439 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:3439 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs181556461	chr7:118646679-118646680	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs146429499	chr7:118646704-118646705	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs566951213	chr7:118646705-118646706	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs543245618	chr7:118646709-118646710	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs115193517	chr7:118646727-118646728	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs6947555	chr7:118646768-118646769	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs549649941	chr7:118646789-118646790	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs549412367	chr7:118646803-118646804	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs186610725	chr7:118646853-118646854	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs528598543	chr7:118646854-118646855	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs112449099	chr7:118646901-118646902	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs571639939	chr7:118646919-118646920	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs191971594	chr7:118646928-118646929	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs183220406	chr7:118646934-118646935	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs557249595	chr7:118646972-118646973	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs551193999	chr7:118647026-118647027	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs567972732	chr7:118647034-118647035	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs149047029	chr7:118647040-118647041	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs186466724	chr7:118647071-118647072	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs571661154	chr7:118647103-118647104	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs540624173	chr7:118647125-118647126	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs557876766	chr7:118647191-118647192	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs577650781	chr7:118647194-118647195	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs10270095	chr7:118647203-118647204	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs143084333	chr7:118647232-118647233	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs10270202	chr7:118647271-118647272	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs575325317	chr7:118647303-118647304	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs542894412	chr7:118647314-118647315	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs4484624	chr7:118647328-118647329	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs371001559	chr7:118647340-118647341	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs111855979	chr7:118647395-118647396	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs191197012	chr7:118647396-118647397	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs539155166	chr7:118647415-118647416	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs182188515	chr7:118647419-118647420	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs115248160	chr7:118647433-118647434	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs75840441	chr7:118647442-118647443	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs530537650	chr7:118647477-118647478	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs550580693	chr7:118647482-118647483	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs188003622	chr7:118647500-118647501	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs368700755	chr7:118647520-118647521	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs536551827	chr7:118647523-118647524	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs553299118	chr7:118647599-118647600	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs139999800	chr7:118647611-118647612	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs566817356	chr7:118647619-118647620	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs112339920	chr7:118647620-118647621	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs199588093	chr7:118647621-118647622	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs79740081	chr7:118647627-118647628	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs398006012	chr7:118647628-118647629	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs200334845	chr7:118647629-118647630	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs200313834	chr7:118647712-118647713	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

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
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	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
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19401682	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Schizophrenia	21346763	CNVD
Myelofibrosis	22110671	CNVD
Renal cell carcinoma	18194544	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:235 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:118646600-118647800	Enhancers	Fetal Brain Male	brain
2	chr7:118646600-118648400	Enhancers	Fetal Lung	lung
3	chr7:118656800-118657800	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr7:118657000-118657200	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr7:118657000-118657600	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr7:118657000-118657800	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr7:118657000-118657800	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr7:118657200-118657600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
9	chr7:118657200-118657800	Enhancers	H9 Cell Line	embryonic stem cell
10	chr7:118657200-118657800	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr7:118657200-118657800	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr7:118657200-118657800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr7:118657400-118657800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr7:118657600-118657800	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr7:118657800-118666400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr7:118661200-118661400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr7:118666400-118666600	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr7:118677400-118678400	Enhancers	Liver	Liver
19	chr7:118695200-118697000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr7:118695400-118697800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr7:118697000-118697400	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr7:118697200-118697600	Enhancers	Aorta	Aorta
23	chr7:118705200-118705600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr7:118705600-118710200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr7:118708400-118710400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr7:118710200-118710400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr7:118710400-118710600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr7:118710400-118710600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr7:118710400-118710800	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr7:118710400-118711400	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr7:118710600-118710800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr7:118710800-118711400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr7:118710800-118711400	Enhancers	Fetal Lung	lung
34	chr7:118710800-118711800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
35	chr7:118711400-118714000	Weak transcription	HUES48 Cell Line	embryonic stem cell
36	chr7:118711400-118714400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr7:118711800-118712000	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr7:118714000-118714400	Enhancers	H1 Cell Line	embryonic stem cell
39	chr7:118714000-118714400	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr7:118714000-118714600	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr7:118714000-118714800	Enhancers	H9 Cell Line	embryonic stem cell
42	chr7:118714400-118714600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr7:118714600-118715400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr7:118715400-118715600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr7:118722400-118722600	Enhancers	iPS-15b Cell Line	embryonic stem cell
46	chr7:118722600-118724200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
47	chr7:118724200-118724600	Enhancers	iPS-15b Cell Line	embryonic stem cell
48	chr7:118724400-118724800	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr7:118724600-118735200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
50	chr7:118730600-118731000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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