Variant report

Variant	nsv889108
Chromosome Location	chr7:119044579-119177670
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	BACH1	chr7:119122299-119123000	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr7:119122424-119122604	GM12878	blood:	n/a	n/a
3	CCNT2	chr7:119174992-119175057	K562	blood:	n/a	n/a
4	CEBPB	chr7:119112634-119113091	HepG2	liver:	n/a	chr7:119112904-119112913 chr7:119112904-119112913 chr7:119112902-119112915 chr7:119112904-119112913 chr7:119112902-119112913 chr7:119112903-119112914 chr7:119112902-119112915 chr7:119112904-119112913
5	CEBPB	chr7:119078390-119078544	K562	blood:	n/a	chr7:119078478-119078489 chr7:119078476-119078487 chr7:119078476-119078489 chr7:119078478-119078487
6	CEBPB	chr7:119112687-119113157	MCF-7	breast:	n/a	chr7:119112904-119112913 chr7:119112904-119112913 chr7:119112902-119112915 chr7:119112904-119112913 chr7:119112902-119112913 chr7:119112903-119112914 chr7:119112902-119112915 chr7:119112904-119112913
7	CEBPB	chr7:119078319-119078656	HepG2	liver:	n/a	chr7:119078478-119078489 chr7:119078476-119078487 chr7:119078476-119078489 chr7:119078478-119078487
8	CEBPB	chr7:119112736-119113039	H1-hESC	embryonic stem cell:	n/a	chr7:119112904-119112913 chr7:119112904-119112913 chr7:119112902-119112915 chr7:119112904-119112913 chr7:119112902-119112913 chr7:119112903-119112914 chr7:119112902-119112915 chr7:119112904-119112913
9	CEBPB	chr7:119139694-119139733	K562	blood:	n/a	chr7:119139713-119139722
10	CEBPB	chr7:119158599-119158739	HepG2	liver:	n/a	chr7:119158656-119158667
11	CEBPB	chr7:119055965-119055997	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr7:119152429-119152660	HepG2	liver:	n/a	chr7:119152514-119152525
13	CEBPB	chr7:119078338-119078628	A549	lung:	n/a	chr7:119078478-119078489 chr7:119078476-119078487 chr7:119078476-119078489 chr7:119078478-119078487
14	CEBPB	chr7:119112798-119112948	HepG2	liver:	n/a	chr7:119112904-119112913 chr7:119112904-119112913 chr7:119112902-119112915 chr7:119112904-119112913 chr7:119112902-119112913 chr7:119112903-119112914 chr7:119112902-119112915 chr7:119112904-119112913
15	CEBPB	chr7:119112723-119113013	A549	lung:	n/a	chr7:119112904-119112913 chr7:119112904-119112913 chr7:119112902-119112915 chr7:119112904-119112913 chr7:119112902-119112913 chr7:119112903-119112914 chr7:119112902-119112915 chr7:119112904-119112913
16	CEBPB	chr7:119112604-119113132	HCT-116	colon:	n/a	chr7:119112904-119112913 chr7:119112904-119112913 chr7:119112902-119112915 chr7:119112904-119112913 chr7:119112902-119112913 chr7:119112903-119112914 chr7:119112902-119112915 chr7:119112904-119112913
17	CEBPB	chr7:119112667-119113038	MCF-7	breast:	n/a	chr7:119112904-119112913 chr7:119112904-119112913 chr7:119112902-119112915 chr7:119112904-119112913 chr7:119112902-119112913 chr7:119112903-119112914 chr7:119112902-119112915 chr7:119112904-119112913
18	CEBPB	chr7:119112600-119113033	HCT-116	colon:	n/a	chr7:119112904-119112913 chr7:119112904-119112913 chr7:119112902-119112915 chr7:119112904-119112913 chr7:119112902-119112913 chr7:119112903-119112914 chr7:119112902-119112915 chr7:119112904-119112913
19	CEBPB	chr7:119112731-119113061	K562	blood:	n/a	chr7:119112904-119112913 chr7:119112904-119112913 chr7:119112902-119112915 chr7:119112904-119112913 chr7:119112902-119112913 chr7:119112903-119112914 chr7:119112902-119112915 chr7:119112904-119112913
20	CEBPB	chr7:119112728-119113065	IMR90	lung:	n/a	chr7:119112904-119112913 chr7:119112904-119112913 chr7:119112902-119112915 chr7:119112904-119112913 chr7:119112902-119112913 chr7:119112903-119112914 chr7:119112902-119112915 chr7:119112904-119112913
21	CEBPB	chr7:119078392-119078635	IMR90	lung:	n/a	chr7:119078478-119078489 chr7:119078476-119078487 chr7:119078476-119078489 chr7:119078478-119078487
22	CHD1	chr7:119083449-119083466	GM12878	blood:	n/a	n/a
23	CTCF	chr7:119122412-119122538	GM10266	blood:	n/a	n/a
24	CTCF	chr7:119122400-119122550	HRPEpiC	eye:	n/a	n/a
25	CTCF	chr7:119122360-119122510	GM12868	blood:	n/a	n/a
26	CTCF	chr7:119122400-119122550	HPF	lung:	n/a	n/a
27	CTCF	chr7:119122080-119122230	HEK293	kidney:	n/a	n/a
28	CTCF	chr7:119141241-119141291	MCF-7	breast:	n/a	n/a
29	CTCF	chr7:119122364-119122549	A549	lung:	n/a	n/a
30	CTCF	chr7:119122368-119122533	GM19240	blood:	n/a	n/a
31	CTCF	chr7:119122440-119122590	HUVEC	blood vessel:	n/a	n/a
32	CTCF	chr7:119122340-119122490	A549	lung:	n/a	n/a
33	CTCF	chr7:119122400-119122550	GM12870	blood:	n/a	n/a
34	CTCF	chr7:119122419-119122540	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr7:119122321-119122544	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr7:119122400-119122550	NB4	blood:	n/a	n/a
37	CTCF	chr7:119122388-119122569	HepG2	liver:	n/a	n/a
38	CTCF	chr7:119122380-119122530	GM12871	blood:	n/a	n/a
39	CTCF	chr7:119122360-119122510	MCF-7	breast:	n/a	n/a
40	CTCF	chr7:119122350-119122558	Medullo	brain:	n/a	n/a
41	CTCF	chr7:119122380-119122530	GM12874	blood:	n/a	n/a
42	CTCF	chr7:119122380-119122530	HPAF	blood vessel:	n/a	n/a
43	CTCF	chr7:119122360-119122510	K562	blood:	n/a	n/a
44	CTCF	chr7:119122380-119122530	GM12864	blood:	n/a	n/a
45	CTCF	chr7:119122400-119122550	NHEK	skin:	n/a	n/a
46	CTCF	chr7:119122170-119122608	MCF-7	breast:	n/a	n/a
47	CTCF	chr7:119122380-119122530	HEEpiC	esophagus:	n/a	n/a
48	CTCF	chr7:119122380-119122530	GM06990	blood:	n/a	n/a
49	CTCF	chr7:119121960-119122110	GM12875	blood:	n/a	n/a
50	CTCF	chr7:119122420-119122570	A549	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:119175916-119175966	MCF-7	breast:	n/a
2	chr7:119175916-119175966	Hela-S3	cervix:	n/a
3	chr7:119121235-119121285	GM12878	blood:	n/a
4	chr7:119175916-119175966	HCF	heart:	n/a
5	chr7:119121235-119121285	HEEpiC	esophagus:	n/a
6	chr7:119175916-119175966	ovcar-3	ovarian:	n/a
7	chr7:119121235-119121285	AG04449	skin:	fetal
8	chr7:119175916-119175966	NHDF-neo	bronchial:	n/a
9	chr7:119175916-119175966	ProgFib	skin:	n/a
10	chr7:119175916-119175966	SK-N-MC	brain:	n/a
11	chr7:119175916-119175966	A549	lung:	n/a
12	chr7:119175916-119175966	U87	brain:	n/a
13	chr7:119175916-119175966	AG09309	skin:	n/a
14	chr7:119121235-119121285	PrEC	prostate:	n/a
15	chr7:119175916-119175966	ECC-1	luminal epithelium:	n/a
16	chr7:119121235-119121285	GM19239	blood:	n/a
17	chr7:119121235-119121285	ovcar-3	ovarian:	n/a
18	chr7:119175916-119175966	AG04449	skin:	fetal
19	chr7:119121235-119121285	ProgFib	skin:	n/a
20	chr7:119121235-119121285	A549	lung:	n/a
21	chr7:119121235-119121285	BJ	skin:	n/a
22	chr7:119121235-119121285	AG09309	skin:	n/a
23	chr7:119175916-119175966	NT2-D1	testis:	n/a
24	chr7:119175916-119175966	HPAEpiC	pulmonary alveolar:	n/a
25	chr7:119175916-119175966	CMK	blood:	n/a
26	chr7:119175916-119175966	Hepatocyte	liver:	n/a
27	chr7:119175916-119175966	AoSMC	blood vessel:	n/a
28	chr7:119121235-119121285	HAEpiC	amniotic membrane:	n/a
29	chr7:119121235-119121285	NHBE	bronchial:	n/a
30	chr7:119121235-119121285	NH-A	brain:	n/a
31	chr7:119175916-119175966	NH-A	brain:	n/a
32	chr7:119121235-119121285	HNPCEpiC	eye:	n/a
33	chr7:119121235-119121285	SKMC	muscle:	n/a
34	chr7:119175916-119175966	HCT-116	colon:	n/a
35	chr7:119121235-119121285	HepG2	liver:	n/a
36	chr7:119175916-119175966	HL-60	blood:	n/a
37	chr7:119121235-119121285	HEK293	kidney:	embryo
38	chr7:119121235-119121285	HPAEpiC	pulmonary alveolar:	n/a
39	chr7:119121235-119121285	H1-hESC	embryonic stem cell:	embryo
40	chr7:119175916-119175966	HEEpiC	esophagus:	n/a
41	chr7:119175916-119175966	T-47D	breast:	n/a
42	chr7:119175916-119175966	RPTEC	kidney:	n/a
43	chr7:119121235-119121285	GM12892	blood:	n/a
44	chr7:119121235-119121285	BE2_C	brain:	n/a
45	chr7:119175916-119175966	Jurkat	blood:	n/a
46	chr7:119175916-119175966	GM12878	blood:	n/a
47	chr7:119175916-119175966	BE2_C	brain:	n/a
48	chr7:119121235-119121285	Caco-2	colon:	n/a
49	chr7:119121235-119121285	PFSK-1	brain:	n/a
50	chr7:119121235-119121285	SK-N-SH	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:119090133..119091662-chr7:119125393..119128092,2	K562	blood:
2	chr6:81998528..81999232-chr7:119153061..119154054,2	MCF-7	breast:
3	chr7:119055228..119059267-chr7:119060829..119064124,3	K562	blood:
4	chr7:119174664..119177243-chr7:119179086..119181541,2	K562	blood:
5	chr7:119090628..119092465-chr7:119234986..119236766,2	K562	blood:
6	chr7:119119277..119121222-chr7:119136610..119138824,2	K562	blood:
7	chr7:119092010..119093559-chr7:119096407..119098268,2	K562	blood:
8	chr7:119101385..119103050-chr7:119105094..119106649,2	K562	blood:
9	chr7:119114137..119115777-chr7:119118248..119120055,2	K562	blood:
10	chr7:119100295..119103050-chr7:119105149..119106900,2	K562	blood:
11	chr7:119057102..119059266-chr7:119065046..119067833,2	K562	blood:
12	chr7:119088296..119090701-chr7:119093018..119094825,2	K562	blood:
13	chr7:119119277..119121222-chr7:119136610..119138824,2	K562	blood:
14	chr7:119090473..119092463-chr7:119095710..119098543,2	MCF-7	breast:
15	chr7:119090133..119091662-chr7:119125393..119128092,2	K562	blood:
16	chr7:119119681..119121337-chr7:119126080..119128108,2	K562	blood:
17	chr7:119100295..119103050-chr7:119105149..119106900,2	K562	blood:
18	chr7:119171216..119174031-chr7:119180101..119182290,2	K562	blood:
19	chr7:119092010..119093559-chr7:119096407..119098268,2	K562	blood:
20	chr7:119055228..119059267-chr7:119060829..119064124,3	K562	blood:
21	chr7:119057102..119059266-chr7:119065046..119067833,2	K562	blood:
22	chr7:119119681..119121337-chr7:119126080..119128108,2	K562	blood:
23	chr7:119088296..119090701-chr7:119093018..119094825,2	K562	blood:
24	chr7:119090473..119092463-chr7:119095710..119098543,2	MCF-7	breast:
25	chr7:119114137..119115777-chr7:119118248..119120055,2	K562	blood:
26	chr7:119101385..119103050-chr7:119105094..119106649,2	K562	blood:

Variant related genes	Relation type
ENSG00000263692	TF binding region
ENSG00000263692	CpG island

Extended variants
information (count: 581 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:581 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7798719	chr7:119044579-119044580	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs532061221	chr7:119044586-119044587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs563609229	chr7:119044588-119044589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs531757599	chr7:119044606-119044607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs549511384	chr7:119044615-119044616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs145286624	chr7:119044622-119044623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs544382338	chr7:119044636-119044637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs559692083	chr7:119044665-119044666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs561096788	chr7:119044721-119044722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs528726060	chr7:119044748-119044749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs547162074	chr7:119044828-119044829	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs201841542	chr7:119044837-119044838	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs11455776	chr7:119044838-119044839	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs397889679	chr7:119044845-119044846	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs570556014	chr7:119044846-119044847	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs546934150	chr7:119044855-119044856	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs539414443	chr7:119044875-119044876	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs370210219	chr7:119044909-119044910	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs549818462	chr7:119044915-119044916	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs73209854	chr7:119044951-119044952	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs137980374	chr7:119044973-119044974	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs555679425	chr7:119044985-119044986	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs149046288	chr7:119044986-119044987	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs143083301	chr7:119045003-119045004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs534851518	chr7:119045018-119045019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs116362841	chr7:119045346-119045347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs148236735	chr7:119045429-119045430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs7803913	chr7:119045448-119045449	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs551934000	chr7:119045467-119045468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs115958360	chr7:119045505-119045506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs12164101	chr7:119045622-119045623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs183227248	chr7:119045630-119045631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs375166052	chr7:119045686-119045687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs142815744	chr7:119045714-119045715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs186943148	chr7:119045772-119045773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs147427672	chr7:119045773-119045774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs191580296	chr7:119045839-119045840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs183932536	chr7:119046040-119046041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs551973673	chr7:119046078-119046079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs118112597	chr7:119046087-119046088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs533069241	chr7:119046090-119046091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs549749746	chr7:119046101-119046102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs565487952	chr7:119046121-119046122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs6972343	chr7:119046180-119046181	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs142998191	chr7:119046181-119046182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs187947366	chr7:119046277-119046278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs192618975	chr7:119046283-119046284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs534487746	chr7:119046343-119046344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs557944627	chr7:119046383-119046384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs147445608	chr7:119046387-119046388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
Myelofibrosis	22110671	CNVD
Renal cell carcinoma	18194544	CNVD
Schizophrenia	23813976	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164919	CNVD

Chromatin state (count:41 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:119044000-119046800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr7:119044800-119045000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr7:119048200-119048800	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr7:119048200-119049400	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr7:119061600-119062200	Enhancers	Liver	Liver
6	chr7:119089600-119090000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr7:119112400-119112600	Active TSS	Liver	Liver
8	chr7:119112400-119112600	Enhancers	Fetal Intestine Large	intestine
9	chr7:119112400-119112800	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr7:119112600-119112800	Flanking Active TSS	Liver	Liver
11	chr7:119112600-119112800	Enhancers	Pancreas	Pancrea
12	chr7:119112600-119113000	Flanking Active TSS	Fetal Intestine Large	intestine
13	chr7:119112600-119113000	Enhancers	Pancreatic Islets	Pancreatic Islet
14	chr7:119112800-119113000	Enhancers	Liver	Liver
15	chr7:119113000-119113200	Enhancers	Fetal Intestine Large	intestine
16	chr7:119117600-119118000	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr7:119118000-119122200	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chr7:119120800-119121200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr7:119122000-119122400	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr7:119122000-119122400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr7:119122000-119123000	Enhancers	H1 Cell Line	embryonic stem cell
22	chr7:119122000-119123600	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr7:119122200-119122400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr7:119122200-119122800	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr7:119122200-119123000	Enhancers	H9 Cell Line	embryonic stem cell
26	chr7:119122200-119123000	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr7:119122200-119123000	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr7:119122200-119123000	Enhancers	Liver	Liver
29	chr7:119122200-119123200	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr7:119123000-119123400	Weak transcription	H9 Cell Line	embryonic stem cell
31	chr7:119133400-119134400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr7:119134400-119135400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr7:119135400-119135800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr7:119154400-119155600	Enhancers	Liver	Liver
35	chr7:119173400-119175200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
36	chr7:119174600-119174800	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr7:119174800-119175400	Weak transcription	HUES6 Cell Line	embryonic stem cell
38	chr7:119174800-119175800	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr7:119175200-119175600	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr7:119175400-119176000	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr7:119175600-119176000	Enhancers	iPS-18 Cell Line	embryonic stem cell

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