Variant report

Variant	nsv889099
Chromosome Location	chr7:118709754-118868426
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:681)
CpG islands
(count:61)
Chromatin interactive
region (count:27)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:681 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr7:118838082-118838260	GM12878	blood:	n/a	n/a
2	BHLHE40	chr7:118816087-118816420	GM12878	blood:	n/a	n/a
3	BRCA1	chr7:118747696-118747725	GM12878	blood:	n/a	n/a
4	CBX3	chr7:118807512-118807928	HCT-116	colon:	n/a	n/a
5	CCNT2	chr7:118787886-118788025	K562	blood:	n/a	n/a
6	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
7	CEBPB	chr7:118742621-118742863	A549	lung:	n/a	chr7:118742808-118742821 chr7:118742809-118742820 chr7:118742808-118742821
8	CEBPB	chr7:118863994-118864177	A549	lung:	n/a	chr7:118864117-118864128
9	CEBPB	chr7:118843922-118844229	IMR90	lung:	n/a	chr7:118844087-118844098 chr7:118844088-118844097 chr7:118844086-118844097
10	CEBPB	chr7:118766145-118766405	HepG2	liver:	n/a	n/a
11	CEBPB	chr7:118730966-118731278	Hela-S3	cervix:	n/a	chr7:118731238-118731251
12	CEBPB	chr7:118840953-118841173	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr7:118850456-118850714	HepG2	liver:	n/a	chr7:118850600-118850611
14	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
15	CEBPB	chr7:118863977-118864186	HepG2	liver:	n/a	chr7:118864117-118864128
16	CEBPB	chr7:118742647-118742847	HepG2	liver:	n/a	chr7:118742808-118742821 chr7:118742809-118742820 chr7:118742808-118742821
17	CEBPB	chr7:118863979-118864179	H1-hESC	embryonic stem cell:	n/a	chr7:118864117-118864128
18	CEBPB	chr7:118843968-118844253	HepG2	liver:	n/a	chr7:118844087-118844098 chr7:118844088-118844097 chr7:118844086-118844097
19	CEBPB	chr7:118843973-118844155	A549	lung:	n/a	chr7:118844087-118844098 chr7:118844088-118844097 chr7:118844086-118844097
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	chr7:118816180-118816330	HCPEpiC	choroid plexus:	n/a	n/a
23	CTCF	chr7:118816200-118816350	GM12874	blood:	n/a	n/a
24	CTCF	chr7:118837340-118837490	GM12875	blood:	n/a	n/a
25	CTCF	chr7:118838100-118838250	SK-N-SH_RA	brain:	n/a	n/a
26	CTCF	chr7:118837796-118838390	GM12878	blood:	n/a	n/a
27	CTCF	chr7:118838120-118838270	AoAF	blood vessel:	n/a	n/a
28	CTCF	chr7:118838080-118838230	AG10803	skin:	n/a	n/a
29	CTCF	chr7:118816160-118816310	GM12867	blood:	n/a	n/a
30	CTCF	chr7:118838055-118838298	A549	lung:	n/a	n/a
31	CTCF	chr7:118838120-118838270	HVMF	connective:	n/a	n/a
32	CTCF	chr7:118838060-118838210	HCT-116	colon:	n/a	n/a
33	CTCF	chr7:118838056-118838293	GM13976	blood:	n/a	n/a
34	CTCF	chr7:118838093-118838243	Lung_OC	lung:	n/a	n/a
35	CTCF	chr7:118816062-118816064	Gliobla	brain:	n/a	n/a
36	CTCF	chr7:118816109-118816426	Medullo	brain:	n/a	n/a
37	CTCF	chr7:118816220-118816370	NHLF	lung:	n/a	n/a
38	CTCF	chr7:118816172-118816283	MCF-7	breast:	n/a	n/a
39	CTCF	chr7:118838140-118838290	HCT-116	colon:	n/a	n/a
40	CTCF	chr7:118837740-118837890	HRE	kidney:	n/a	n/a
41	CTCF	chr7:118838100-118838250	GM12869	blood:	n/a	n/a
42	CTCF	chr7:118864080-118864111	ProgFib	skin:	n/a	n/a
43	CTCF	chr7:118837640-118837790	WERI-Rb-1	eye:	n/a	n/a
44	CTCF	chr7:118816162-118816262	GM12891	blood:	n/a	n/a
45	CTCF	chr7:118837480-118837630	GM12865	blood:	n/a	n/a
46	CTCF	chr7:118838060-118838210	NHEK	skin:	n/a	n/a
47	CTCF	chr7:118754000-118754150	GM12871	blood:	n/a	n/a
48	CTCF	chr7:118838100-118838250	AG04449	skin:	n/a	n/a
49	CTCF	chr7:118816220-118816370	GM12866	blood:	n/a	n/a
50	CTCF	chr7:118816180-118816330	HPAF	blood vessel:	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	AG04449	skin:	fetal
2	chr7:118741415-118741465	AoSMC	blood vessel:	n/a
3	chr7:118741415-118741465	HRPEpiC	eye:	n/a
4	chr7:118741415-118741465	HL-60	blood:	n/a
5	chr7:118741415-118741465	HNPCEpiC	eye:	n/a
6	chr7:118741415-118741465	HRCEpiC	kidney:	n/a
7	chr7:118741415-118741465	HPAEpiC	pulmonary alveolar:	n/a
8	chr7:118741415-118741465	RPTEC	kidney:	n/a
9	chr7:118741415-118741465	HIPEpiC	eye:	n/a
10	chr7:118741415-118741465	HRE	kidney:	n/a
11	chr7:118741415-118741465	CMK	blood:	n/a
12	chr7:118741415-118741465	LNCaP	prostate:	n/a
13	chr7:118741415-118741465	GM06990	blood:	n/a
14	chr7:118741415-118741465	HCF	heart:	n/a
15	chr7:118741415-118741465	AG04450	lung:	fetal
16	chr7:118741415-118741465	PFSK-1	brain:	n/a
17	chr7:118741415-118741465	HAEpiC	amniotic membrane:	n/a
18	chr7:118741415-118741465	SK-N-MC	brain:	n/a
19	chr7:118741415-118741465	NH-A	brain:	n/a
20	chr7:118741415-118741465	HCT-116	colon:	n/a
21	chr7:118741415-118741465	MCF10A-Er-Src	breast:	n/a
22	chr7:118741415-118741465	ovcar-3	ovarian:	n/a
23	chr7:118741415-118741465	NB4	blood:	n/a
24	chr7:118741415-118741465	BE2_C	brain:	n/a
25	chr7:118741415-118741465	A549	lung:	n/a
26	chr7:118741415-118741465	GM12891	blood:	n/a
27	chr7:118741415-118741465	MCF-7	breast:	n/a
28	chr7:118741415-118741465	NHDF-neo	bronchial:	n/a
29	chr7:118741415-118741465	NHBE	bronchial:	n/a
30	chr7:118741415-118741465	ECC-1	luminal epithelium:	n/a
31	chr7:118741415-118741465	Caco-2	colon:	n/a
32	chr7:118741415-118741465	SAEC	small airway:	n/a
33	chr7:118741415-118741465	SK-N-SH_RA	brain:	n/a
34	chr7:118741415-118741465	ProgFib	skin:	n/a
35	chr7:118741415-118741465	U87	brain:	n/a
36	chr7:118741415-118741465	Hela-S3	cervix:	n/a
37	chr7:118741415-118741465	IMR90	lung:	fetal
38	chr7:118741415-118741465	Hepatocyte	liver:	n/a
39	chr7:118741415-118741465	T-47D	breast:	n/a
40	chr7:118741415-118741465	K562	blood:	n/a
41	chr7:118741415-118741465	SKMC	muscle:	n/a
42	chr7:118741415-118741465	Jurkat	blood:	n/a
43	chr7:118741415-118741465	GM19239	blood:	n/a
44	chr7:118741415-118741465	HMEC	breast:	n/a
45	chr7:118741415-118741465	BJ	skin:	n/a
46	chr7:118741415-118741465	HEK293	kidney:	embryo
47	chr7:118741415-118741465	SK-N-SH	brain:	n/a
48	chr7:118741415-118741465	AG09319	gingival:	n/a
49	chr7:118741415-118741465	HepG2	liver:	n/a
50	chr7:118741415-118741465	NT2-D1	testis:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:118800323..118802977-chr7:118807126..118809160,2	K562	blood:
2	chr7:118829678..118832309-chr7:118833350..118835537,2	MCF-7	breast:
3	chr7:118629006..118631002-chr7:118732998..118734533,2	K562	blood:
4	chr7:118829678..118832309-chr7:118833350..118835537,2	MCF-7	breast:
5	chr6:30580881..30583485-chr7:118868073..118870261,2	MCF-7	breast:
6	chr7:117992651..117993374-chr7:118815864..118816654,2	MCF-7	breast:
7	chr7:118852197..118855111-chr7:118862886..118865559,2	K562	blood:
8	chr7:118782215..118784443-chr7:118786067..118788168,2	K562	blood:
9	chr7:118558392..118559287-chr7:118815693..118816489,5	MCF-7	breast:
10	chr7:118823416..118825410-chr7:118825629..118827229,2	K562	blood:
11	chr7:118733515..118736474-chr7:118742172..118744304,2	K562	blood:
12	chr7:118742557..118744399-chr7:118756096..118757786,2	K562	blood:
13	chr7:118733515..118736474-chr7:118742172..118744304,2	K562	blood:
14	chr7:118510382..118510908-chr7:118815972..118816682,2	MCF-7	breast:
15	chr7:118558904..118559746-chr7:118816086..118816731,2	MCF-7	breast:
16	chr7:118792620..118793489-chr9:140473359..140473903,2	Hela-S3	cervix:
17	chr7:118288299..118289194-chr7:118816171..118816706,2	MCF-7	breast:
18	chr7:118742557..118744399-chr7:118756096..118757786,2	K562	blood:
19	chr7:118852197..118855111-chr7:118862886..118865559,2	K562	blood:
20	chr7:118800323..118802977-chr7:118807126..118809160,2	K562	blood:
21	chr7:117390803..117391431-chr7:118815895..118816706,2	MCF-7	breast:
22	chr7:118857357..118859002-chr8:11343082..11345568,2	MCF-7	breast:
23	chr7:117992682..117993833-chr7:118815599..118816513,3	MCF-7	breast:
24	chr7:118558340..118559254-chr7:118837696..118838683,4	MCF-7	breast:
25	chr7:118823416..118825410-chr7:118825629..118827229,2	K562	blood:
26	chr7:117992579..117993168-chr7:118815740..118816656,2	K562	blood:
27	chr7:118782215..118784443-chr7:118786067..118788168,2	K562	blood:

(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: 2688 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:2688 , 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	rs10238286	chr7:118709754-118709755	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs10238297	chr7:118709801-118709802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs184199286	chr7:118709846-118709847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs562277941	chr7:118709888-118709889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs78012857	chr7:118709975-118709976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs11984303	chr7:118709978-118709979	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs376994959	chr7:118710045-118710046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs541318823	chr7:118710050-118710051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs566603697	chr7:118710075-118710076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs564183752	chr7:118710109-118710110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs577505046	chr7:118710164-118710165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs117032409	chr7:118710189-118710190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs11974339	chr7:118710197-118710198	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs75851029	chr7:118710223-118710224	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs549175513	chr7:118710320-118710321	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs549223351	chr7:118710338-118710339	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs559918661	chr7:118710369-118710370	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs143388307	chr7:118710465-118710466	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs148365461	chr7:118710466-118710467	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs12706220	chr7:118710524-118710525	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs113433186	chr7:118710548-118710549	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs531230759	chr7:118710611-118710612	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs368132798	chr7:118710726-118710727	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs549832909	chr7:118710728-118710729	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs147344000	chr7:118710757-118710758	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs535555660	chr7:118710784-118710785	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs555119425	chr7:118710850-118710851	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs368185220	chr7:118710874-118710875	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs534553676	chr7:118710910-118710911	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs557928019	chr7:118710932-118710933	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs200778233	chr7:118710933-118710934	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs543297058	chr7:118710967-118710968	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs556952032	chr7:118711081-118711082	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs573671468	chr7:118711117-118711118	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs538533731	chr7:118711151-118711152	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs543112143	chr7:118711152-118711153	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs559548728	chr7:118711155-118711156	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs77933052	chr7:118711193-118711194	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs375315949	chr7:118711202-118711203	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs188836445	chr7:118711213-118711214	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs531268510	chr7:118711224-118711225	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs551265158	chr7:118711249-118711250	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs569670249	chr7:118711269-118711270	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs75879265	chr7:118711270-118711271	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs137945243	chr7:118711297-118711298	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs565683906	chr7:118711300-118711301	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs534692388	chr7:118711317-118711318	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs11979165	chr7:118711335-118711336	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs116166618	chr7:118711359-118711360	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs76340802	chr7:118711371-118711372	Enhancers Weak transcription	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:212 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:118705600-118710200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr7:118708400-118710400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr7:118710200-118710400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr7:118710400-118710600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr7:118710400-118710600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr7:118710400-118710800	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr7:118710400-118711400	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr7:118710600-118710800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr7:118710800-118711400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr7:118710800-118711400	Enhancers	Fetal Lung	lung
11	chr7:118710800-118711800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr7:118711400-118714000	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr7:118711400-118714400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr7:118711800-118712000	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr7:118714000-118714400	Enhancers	H1 Cell Line	embryonic stem cell
16	chr7:118714000-118714400	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr7:118714000-118714600	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr7:118714000-118714800	Enhancers	H9 Cell Line	embryonic stem cell
19	chr7:118714400-118714600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr7:118714600-118715400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr7:118715400-118715600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr7:118722400-118722600	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr7:118722600-118724200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
24	chr7:118724200-118724600	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr7:118724400-118724800	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr7:118724600-118735200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
27	chr7:118730600-118731000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr7:118735400-118740600	Weak transcription	Pancreatic Islets	Pancreatic Islet
29	chr7:118736000-118736200	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
30	chr7:118736200-118739800	Weak transcription	H9 Cell Line	embryonic stem cell
31	chr7:118739000-118739200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr7:118739200-118739800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr7:118739200-118740200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr7:118739200-118743200	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr7:118739400-118740800	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr7:118739600-118740600	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr7:118739600-118740800	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr7:118739800-118740600	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr7:118739800-118740800	Enhancers	H9 Cell Line	embryonic stem cell
40	chr7:118739800-118741400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr7:118740000-118742800	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr7:118740200-118740600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr7:118740200-118740600	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr7:118740600-118740800	Enhancers	H1 Cell Line	embryonic stem cell
45	chr7:118740600-118740800	Enhancers	Pancreatic Islets	Pancreatic Islet
46	chr7:118740600-118740800	Enhancers	Fetal Lung	lung
47	chr7:118740600-118741000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
48	chr7:118740600-118741000	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
49	chr7:118740600-118741000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
50	chr7:118740600-118741000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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