Variant report

Variant	nsv608067
Chromosome Location	chr7:103944237-104029408
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:331)
CpG islands
(count:610)
Chromatin interactive
region (count:31)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:331 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr7:103968592-103968706	H1-hESC	embryonic stem cell:	n/a	n/a
2	CBX3	chr7:104028640-104029043	K562	blood:	n/a	n/a
3	CBX3	chr7:104028733-104029024	K562	blood:	n/a	n/a
4	CEBPB	chr7:103970126-103970472	A549	lung:	n/a	chr7:103970276-103970293
5	CEBPB	chr7:103970064-103970537	MCF-7	breast:	n/a	chr7:103970276-103970293
6	CEBPB	chr7:104003887-104004243	MCF-7	breast:	n/a	chr7:104004064-104004075
7	CEBPB	chr7:104010194-104010275	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr7:103970139-103970464	K562	blood:	n/a	chr7:103970276-103970293
9	CEBPB	chr7:103970145-103970441	IMR90	lung:	n/a	chr7:103970276-103970293
10	CEBPB	chr7:104003966-104004143	HepG2	liver:	n/a	chr7:104004064-104004075
11	CEBPB	chr7:103958334-103958416	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr7:103970111-103970444	H1-hESC	embryonic stem cell:	n/a	chr7:103970276-103970293
13	CEBPB	chr7:103968427-103968764	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr7:103970123-103970461	HepG2	liver:	n/a	chr7:103970276-103970293
15	CEBPB	chr7:103979722-103979904	HepG2	liver:	n/a	n/a
16	CEBPB	chr7:104003836-104004188	H1-hESC	embryonic stem cell:	n/a	chr7:104004064-104004075
17	CEBPB	chr7:103977684-103977884	HepG2	liver:	n/a	chr7:103977737-103977748 chr7:103977768-103977779
18	CEBPB	chr7:103970167-103970444	Hela-S3	cervix:	n/a	chr7:103970276-103970293
19	CEBPB	chr7:103977739-103977757	K562	blood:	n/a	n/a
20	CEBPB	chr7:103995080-103995352	HepG2	liver:	n/a	chr7:103995227-103995238
21	CEBPB	chr7:103968594-103968649	HepG2	liver:	n/a	n/a
22	CEBPB	chr7:103995147-103995309	A549	lung:	n/a	chr7:103995227-103995238
23	CTBP2	chr7:103969402-103970172	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr7:103982160-103982310	GM06990	blood:	n/a	chr7:103982189-103982207
25	CTCF	chr7:103982100-103982250	BE2_C	brain:	n/a	chr7:103982189-103982207
26	CTCF	chr7:103982040-103982190	GM12873	blood:	n/a	n/a
27	CTCF	chr7:103982054-103982312	MCF-7	breast:	n/a	chr7:103982189-103982207
28	CTCF	chr7:103982080-103982230	Hela-S3	cervix:	n/a	chr7:103982189-103982207
29	CTCF	chr7:103982120-103982270	A549	lung:	n/a	chr7:103982189-103982207
30	CTCF	chr7:103982162-103982212	NHEK	skin:	n/a	chr7:103982189-103982207
31	CTCF	chr7:103982093-103982308	HepG2	liver:	n/a	chr7:103982189-103982207
32	CTCF	chr7:103998161-103998189	Hela-S3	cervix:	n/a	n/a
33	CTCF	chr7:103950948-103950984	GM10248	blood:	n/a	n/a
34	CTCF	chr7:103982180-103982330	HCT-116	colon:	n/a	chr7:103982189-103982207
35	CTCF	chr7:103982120-103982270	GM12875	blood:	n/a	chr7:103982189-103982207
36	CTCF	chr7:103982080-103982230	HMF	breast:	n/a	chr7:103982189-103982207
37	CTCF	chr7:103981979-103982321	H1-hESC	embryonic stem cell:	n/a	chr7:103982189-103982207
38	CTCF	chr7:103982120-103982270	HepG2	liver:	n/a	chr7:103982189-103982207
39	CTCF	chr7:103998100-103998250	MCF-7	breast:	n/a	n/a
40	CTCF	chr7:103982116-103982301	LNCaP	prostate:	n/a	chr7:103982189-103982207
41	CTCF	chr7:104018692-104018719	GM13976	blood:	n/a	n/a
42	CTCF	chr7:103982080-103982230	GM12875	blood:	n/a	chr7:103982189-103982207
43	CTCF	chr7:103982140-103982290	WERI-Rb-1	eye:	n/a	chr7:103982189-103982207
44	CTCF	chr7:103998080-103998230	NHEK	skin:	n/a	n/a
45	CTCF	chr7:103998121-103998241	MCF-7	breast:	n/a	n/a
46	CTCF	chr7:103982200-103982350	HRPEpiC	eye:	n/a	n/a
47	CTCF	chr7:103999280-103999430	GM12869	blood:	n/a	n/a
48	CTCF	chr7:103982120-103982270	HEK293	kidney:	n/a	chr7:103982189-103982207
49	CTCF	chr7:103982200-103982350	HFF-Myc	foreskin:	n/a	n/a
50	CTCF	chr7:103982091-103982285	ProgFib	skin:	n/a	chr7:103982189-103982207

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:103969268-103969318	CMK	blood:	n/a
2	chr7:104004514-104004564	NHDF-neo	bronchial:	n/a
3	chr7:103969166-103969216	GM12892	blood:	n/a
4	chr7:103969483-103969533	AG09309	skin:	n/a
5	chr7:103968795-103968845	LNCaP	prostate:	n/a
6	chr7:103969940-103969990	AG09319	gingival:	n/a
7	chr7:103969940-103969990	HepG2	liver:	n/a
8	chr7:103969268-103969318	HPAEpiC	pulmonary alveolar:	n/a
9	chr7:103968795-103968845	CMK	blood:	n/a
10	chr7:103968615-103968665	NH-A	brain:	n/a
11	chr7:104004514-104004564	A549	lung:	n/a
12	chr7:103969268-103969318	T-47D	breast:	n/a
13	chr7:103969166-103969216	CMK	blood:	n/a
14	chr7:103968795-103968845	ECC-1	luminal epithelium:	n/a
15	chr7:103965666-103965716	HRE	kidney:	n/a
16	chr7:103968615-103968665	AG10803	skin:	n/a
17	chr7:103965666-103965716	HCM	heart:	n/a
18	chr7:103965666-103965716	NH-A	brain:	n/a
19	chr7:103969166-103969216	AoSMC	blood vessel:	n/a
20	chr7:103969940-103969990	GM12878	blood:	n/a
21	chr7:103969268-103969318	HRPEpiC	eye:	n/a
22	chr7:103969268-103969318	HCPEpiC	choroid plexus:	n/a
23	chr7:103969268-103969318	BE2_C	brain:	n/a
24	chr7:103969166-103969216	GM12891	blood:	n/a
25	chr7:103969483-103969533	BE2_C	brain:	n/a
26	chr7:104004514-104004564	T-47D	breast:	n/a
27	chr7:103968615-103968665	Hepatocyte	liver:	n/a
28	chr7:103969268-103969318	BJ	skin:	n/a
29	chr7:104004514-104004564	AG10803	skin:	n/a
30	chr7:103965666-103965716	K562	blood:	n/a
31	chr7:103968615-103968665	RPTEC	kidney:	n/a
32	chr7:103969940-103969990	K562	blood:	n/a
33	chr7:103968795-103968845	HUVEC	blood vessel:	n/a
34	chr7:104004514-104004564	HIPEpiC	eye:	n/a
35	chr7:103969318-103969368	GM12878	blood:	n/a
36	chr7:103969166-103969216	SK-N-SH_RA	brain:	n/a
37	chr7:103969268-103969318	HCM	heart:	n/a
38	chr7:103969940-103969990	CMK	blood:	n/a
39	chr7:104004514-104004564	HEK293	kidney:	embryo
40	chr7:103969318-103969368	Jurkat	blood:	n/a
41	chr7:104004514-104004564	CMK	blood:	n/a
42	chr7:103969318-103969368	GM19239	blood:	n/a
43	chr7:104004514-104004564	SK-N-MC	brain:	n/a
44	chr7:104004514-104004564	U87	brain:	n/a
45	chr7:103965666-103965716	GM12891	blood:	n/a
46	chr7:103970195-103970245	HepG2	liver:	n/a
47	chr7:103969318-103969368	GM06990	blood:	n/a
48	chr7:103965666-103965716	SK-N-SH	brain:	n/a
49	chr7:103969166-103969216	HRPEpiC	eye:	n/a
50	chr7:103969318-103969368	PFSK-1	brain:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:103952166..103954106-chr7:103959256..103961820,2	K562	blood:
2	chr7:104003184..104004099-chr7:104209605..104210719,5	MCF-7	breast:
3	chr7:104003200..104003727-chr7:104210005..104210608,2	MCF-7	breast:
4	chr7:104028797..104030802-chr7:104033440..104036374,2	K562	blood:
5	chr7:104015110..104017343-chr7:104021925..104024838,2	K562	blood:
6	chr7:104009174..104011745-chr7:104015096..104016988,2	K562	blood:
7	chr7:104015192..104017343-chr7:104023338..104025477,2	K562	blood:
8	chr7:103982169..103982671-chr7:104502639..104503479,2	MCF-7	breast:
9	chr7:104010772..104012610-chr7:104014348..104016173,2	K562	blood:
10	chr7:103981713..103982644-chr7:104488433..104489374,3	MCF-7	breast:
11	chr7:103785594..103788558-chr7:103959562..103962254,2	K562	blood:
12	chr7:103847182..103849420-chr7:103988053..103990477,2	MCF-7	breast:
13	chr7:104002035..104004913-chr7:104011851..104013907,2	MCF-7	breast:
14	chr7:103929923..103932419-chr7:103948593..103951265,2	K562	blood:
15	chr7:103994443..103997481-chr7:104000926..104004023,3	K562	blood:
16	chr7:103952166..103954106-chr7:103959256..103961820,2	K562	blood:
17	chr7:104005490..104008037-chr7:104011200..104013978,2	K562	blood:
18	chr7:104006537..104008285-chr7:104010089..104012700,2	K562	blood:
19	chr7:104006537..104008285-chr7:104010089..104012700,2	K562	blood:
20	chr7:103958297..103961032-chr7:103966268..103968411,2	K562	blood:
21	chr7:104009174..104011745-chr7:104015096..104016988,2	K562	blood:
22	chr7:104005490..104008037-chr7:104011200..104013978,2	K562	blood:
23	chr7:103957548..103961032-chr7:103963937..103968411,4	K562	blood:
24	chr7:104015338..104017844-chr7:104195492..104197847,2	K562	blood:
25	chr7:104010772..104012610-chr7:104014348..104016173,2	K562	blood:
26	chr7:104002035..104004913-chr7:104011851..104013907,2	MCF-7	breast:
27	chr7:103958297..103961032-chr7:103966268..103968411,2	K562	blood:
28	chr7:104015192..104017343-chr7:104023338..104025477,2	K562	blood:
29	chr7:103957548..103961032-chr7:103963937..103968411,4	K562	blood:
30	chr7:103994443..103997481-chr7:104000926..104004023,3	K562	blood:
31	chr7:104015110..104017343-chr7:104021925..104024838,2	K562	blood:

No data

Variant related genes	Relation type
LHFPL3	TF binding region
LHFPL3	CpG island
ENSG00000164815	chromatin interactions

Extended variants
information (count: 1230 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:1230 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562219931	chr7:103945436-103945437	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs188237026	chr7:103945521-103945522	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs551316823	chr7:103945548-103945549	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs562246015	chr7:103945565-103945566	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs61311662	chr7:103945584-103945585	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs574084612	chr7:103945627-103945628	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs533388933	chr7:103945637-103945638	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs551332185	chr7:103945712-103945713	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs144789169	chr7:103945720-103945721	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs569806316	chr7:103945768-103945769	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs147591237	chr7:103945775-103945776	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs564978207	chr7:103947200-103947201	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs559774194	chr7:103947211-103947212	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs977641	chr7:103947247-103947248	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs547547037	chr7:103947257-103947258	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs565762596	chr7:103947286-103947287	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs148911624	chr7:103947306-103947307	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs199798716	chr7:103947328-103947329	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs77212328	chr7:103947330-103947331	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs397750191	chr7:103947334-103947335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs547844963	chr7:103947369-103947370	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs143590889	chr7:103947370-103947371	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs551858694	chr7:103947371-103947372	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs559280913	chr7:103947423-103947424	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs556813664	chr7:103947454-103947455	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs2028025	chr7:103947460-103947461	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs538826368	chr7:103947493-103947494	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs553869873	chr7:103947531-103947532	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs79283756	chr7:103947592-103947593	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs138099408	chr7:103947601-103947602	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs554618921	chr7:103947623-103947624	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs563348641	chr7:103947635-103947636	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs181790957	chr7:103947642-103947643	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs35116217	chr7:103947646-103947647	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs530677602	chr7:103947708-103947709	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs543390611	chr7:103947721-103947722	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs185208773	chr7:103947762-103947763	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs565159629	chr7:103947763-103947764	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs532379175	chr7:103947798-103947799	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs142576072	chr7:103947799-103947800	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs566568081	chr7:103958204-103958205	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs184510626	chr7:103958238-103958239	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs62489777	chr7:103958270-103958271	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs567304700	chr7:103958303-103958304	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs148239213	chr7:103958307-103958308	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs542647620	chr7:103958322-103958323	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs537819965	chr7:103958388-103958389	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs76445484	chr7:103958391-103958392	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs17389507	chr7:103958408-103958409	Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs540025886	chr7:103958409-103958410	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

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
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	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
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
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Bladder cancer	21909424	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	21858162	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Prostate cancer	18632612	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	19907438	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	20967226	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Basal cell lymphoma	17053054	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:331 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:103945400-103945800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr7:103947200-103947800	Enhancers	Fetal Brain Male	brain
3	chr7:103947400-103947800	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr7:103958200-103958400	Enhancers	H9 Cell Line	embryonic stem cell
5	chr7:103958200-103958400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr7:103958200-103958600	Enhancers	H1 Cell Line	embryonic stem cell
7	chr7:103958200-103958600	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr7:103958200-103958800	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr7:103958200-103959000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr7:103958200-103959000	Enhancers	Cortex derived primary cultured neurospheres	brain
11	chr7:103958200-103959200	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr7:103958200-103959200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr7:103958200-103959400	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr7:103958400-103958600	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
15	chr7:103958400-103958600	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr7:103958400-103958800	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr7:103965800-103966600	Enhancers	NHDF-Ad	bronchial
18	chr7:103966200-103966800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr7:103966600-103968400	Enhancers	Cortex derived primary cultured neurospheres	brain
20	chr7:103968000-103968400	Enhancers	Brain Substantia Nigra	brain
21	chr7:103968200-103968400	Bivalent/Poised TSS	Fetal Brain Male	brain
22	chr7:103968200-103968600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr7:103968200-103968600	Bivalent/Poised TSS	Rectal Mucosa Donor 29	rectum
24	chr7:103968200-103968800	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
25	chr7:103968200-103968800	Flanking Active TSS	Brain Germinal Matrix	brain
26	chr7:103968200-103970200	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
27	chr7:103968200-103970200	Bivalent Enhancer	Fetal Lung	lung
28	chr7:103968200-103970400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
29	chr7:103968400-103968600	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
30	chr7:103968400-103968600	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
31	chr7:103968400-103968600	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr7:103968400-103968600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr7:103968400-103968600	Bivalent Enhancer	Fetal Brain Male	brain
34	chr7:103968400-103968600	Bivalent Enhancer	Fetal Stomach	stomach
35	chr7:103968400-103968800	Bivalent/Poised TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr7:103968400-103968800	Bivalent/Poised TSS	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr7:103968400-103968800	Flanking Bivalent TSS/Enh	Brain Hippocampus Middle	brain
38	chr7:103968400-103968800	Flanking Bivalent TSS/Enh	Fetal Brain Female	brain
39	chr7:103968400-103969000	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
40	chr7:103968400-103969000	Bivalent Enhancer	Fetal Muscle Leg	muscle
41	chr7:103968400-103969200	Enhancers	Pancreas	Pancrea
42	chr7:103968400-103969800	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
43	chr7:103968400-103970400	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
44	chr7:103968400-103970400	Active TSS	Brain Substantia Nigra	brain
45	chr7:103968400-103970600	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
46	chr7:103968400-103971000	Active TSS	Brain Anterior Caudate	brain
47	chr7:103968600-103968800	Flanking Bivalent TSS/Enh	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr7:103968600-103968800	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr7:103968600-103968800	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr7:103968600-103968800	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast

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