Variant report

Variant	nsv888522
Chromosome Location	chr7:79402551-79619012
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	ARID3A	chr7:79444490-79444699	HepG2	liver:	n/a	n/a
2	ATF1	chr7:79477157-79477331	K562	blood:	n/a	n/a
3	BHLHE40	chr7:79579192-79579444	HepG2	liver:	n/a	n/a
4	BRCA1	chr7:79435827-79436050	Hela-S3	cervix:	n/a	n/a
5	CCNT2	chr7:79470384-79470531	K562	blood:	n/a	n/a
6	CEBPB	chr7:79582670-79582684	IMR90	lung:	n/a	n/a
7	CEBPB	chr7:79443801-79444061	K562	blood:	n/a	chr7:79443908-79443919 chr7:79443906-79443919 chr7:79443908-79443917 chr7:79443908-79443917 chr7:79443908-79443917 chr7:79443908-79443917
8	CEBPB	chr7:79498190-79498522	A549	lung:	n/a	chr7:79498350-79498359 chr7:79498350-79498359 chr7:79498350-79498359 chr7:79498349-79498360 chr7:79498348-79498359 chr7:79498350-79498359 chr7:79498348-79498361
9	CEBPB	chr7:79443800-79444019	IMR90	lung:	n/a	chr7:79443908-79443919 chr7:79443906-79443919 chr7:79443908-79443917 chr7:79443908-79443917 chr7:79443908-79443917 chr7:79443908-79443917
10	CEBPB	chr7:79597809-79598002	HepG2	liver:	n/a	n/a
11	CEBPB	chr7:79506305-79506627	A549	lung:	n/a	chr7:79506438-79506449
12	CEBPB	chr7:79447704-79447967	IMR90	lung:	n/a	chr7:79447857-79447868
13	CEBPB	chr7:79523359-79523585	IMR90	lung:	n/a	n/a
14	CEBPB	chr7:79590108-79590447	IMR90	lung:	n/a	chr7:79590268-79590279
15	CEBPB	chr7:79512251-79512607	HepG2	liver:	n/a	chr7:79512419-79512430 chr7:79512456-79512467
16	CEBPB	chr7:79408422-79408658	A549	lung:	n/a	chr7:79408546-79408557
17	CEBPB	chr7:79594189-79594386	HepG2	liver:	n/a	chr7:79594320-79594331 chr7:79594319-79594332
18	CEBPB	chr7:79498324-79498484	H1-hESC	embryonic stem cell:	n/a	chr7:79498350-79498359 chr7:79498350-79498359 chr7:79498350-79498359 chr7:79498349-79498360 chr7:79498348-79498359 chr7:79498350-79498359 chr7:79498348-79498361
19	CEBPB	chr7:79608713-79609150	IMR90	lung:	n/a	n/a
20	CEBPB	chr7:79526164-79526364	IMR90	lung:	n/a	n/a
21	CEBPB	chr7:79452644-79452960	IMR90	lung:	n/a	n/a
22	CEBPB	chr7:79590249-79590302	Hela-S3	cervix:	n/a	chr7:79590268-79590279
23	CEBPB	chr7:79590101-79590424	A549	lung:	n/a	chr7:79590268-79590279
24	CEBPB	chr7:79467299-79467509	H1-hESC	embryonic stem cell:	n/a	chr7:79467438-79467449
25	CEBPB	chr7:79512278-79512607	Hela-S3	cervix:	n/a	chr7:79512419-79512430 chr7:79512456-79512467
26	CEBPB	chr7:79579133-79579419	HepG2	liver:	n/a	chr7:79579253-79579266
27	CEBPB	chr7:79506245-79506640	Hela-S3	cervix:	n/a	chr7:79506438-79506449
28	CEBPB	chr7:79467287-79467586	ECC-1	luminal epithelium:	n/a	chr7:79467438-79467449
29	CEBPB	chr7:79408286-79408736	Hela-S3	cervix:	n/a	chr7:79408546-79408557 chr7:79408298-79408311
30	CEBPB	chr7:79559946-79560240	IMR90	lung:	n/a	n/a
31	CEBPB	chr7:79498199-79498523	IMR90	lung:	n/a	chr7:79498350-79498359 chr7:79498350-79498359 chr7:79498350-79498359 chr7:79498349-79498360 chr7:79498348-79498359 chr7:79498350-79498359 chr7:79498348-79498361
32	CEBPB	chr7:79408123-79408872	IMR90	lung:	n/a	chr7:79408546-79408557 chr7:79408298-79408311
33	CEBPB	chr7:79483878-79484196	IMR90	lung:	n/a	chr7:79484007-79484018
34	CEBPB	chr7:79483994-79484071	HepG2	liver:	n/a	chr7:79484007-79484018
35	CEBPB	chr7:79590191-79590358	MCF-7	breast:	n/a	chr7:79590268-79590279
36	CEBPB	chr7:79537550-79537878	IMR90	lung:	n/a	chr7:79537700-79537713 chr7:79537811-79537822 chr7:79537702-79537711 chr7:79537702-79537711 chr7:79537702-79537711
37	CEBPB	chr7:79443751-79444016	A549	lung:	n/a	chr7:79443908-79443919 chr7:79443906-79443919 chr7:79443908-79443917 chr7:79443908-79443917 chr7:79443908-79443917 chr7:79443908-79443917
38	CEBPB	chr7:79498190-79498519	HepG2	liver:	n/a	chr7:79498350-79498359 chr7:79498350-79498359 chr7:79498350-79498359 chr7:79498349-79498360 chr7:79498348-79498359 chr7:79498350-79498359 chr7:79498348-79498361
39	CEBPB	chr7:79561788-79561825	A549	lung:	n/a	n/a
40	CEBPB	chr7:79537531-79537881	A549	lung:	n/a	chr7:79537700-79537713 chr7:79537811-79537822 chr7:79537702-79537711 chr7:79537702-79537711 chr7:79537702-79537711
41	CEBPB	chr7:79467258-79467600	Hela-S3	cervix:	n/a	chr7:79467438-79467449
42	CEBPB	chr7:79512239-79512609	A549	lung:	n/a	chr7:79512419-79512430 chr7:79512456-79512467
43	CEBPB	chr7:79512269-79512607	A549	lung:	n/a	chr7:79512419-79512430 chr7:79512456-79512467
44	CEBPB	chr7:79590095-79590450	HepG2	liver:	n/a	chr7:79590268-79590279
45	CEBPB	chr7:79526711-79526904	HepG2	liver:	n/a	chr7:79526758-79526769
46	CEBPB	chr7:79498188-79498511	Hela-S3	cervix:	n/a	chr7:79498350-79498359 chr7:79498350-79498359 chr7:79498350-79498359 chr7:79498349-79498360 chr7:79498348-79498359 chr7:79498350-79498359 chr7:79498348-79498361
47	CEBPB	chr7:79512287-79512602	K562	blood:	n/a	chr7:79512419-79512430 chr7:79512456-79512467
48	CEBPB	chr7:79562584-79562882	HepG2	liver:	n/a	chr7:79562758-79562769
49	CEBPB	chr7:79462187-79462387	HepG2	liver:	n/a	n/a
50	CEBPB	chr7:79467263-79467599	HepG2	liver:	n/a	chr7:79467438-79467449

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:79554138-79554188	ECC-1	luminal epithelium:	n/a
2	chr7:79609099-79609149	NB4	blood:	n/a
3	chr7:79554138-79554188	HCPEpiC	choroid plexus:	n/a
4	chr7:79609099-79609149	AG04449	skin:	fetal
5	chr7:79609099-79609149	ProgFib	skin:	n/a
6	chr7:79554138-79554188	SK-N-MC	brain:	n/a
7	chr7:79609099-79609149	PANC-1	pancreas:	n/a
8	chr7:79609099-79609149	ECC-1	luminal epithelium:	n/a
9	chr7:79609099-79609149	SKMC	muscle:	n/a
10	chr7:79554138-79554188	HRCEpiC	kidney:	n/a
11	chr7:79609099-79609149	Hela-S3	cervix:	n/a
12	chr7:79554138-79554188	BE2_C	brain:	n/a
13	chr7:79609099-79609149	AoSMC	blood vessel:	n/a
14	chr7:79554138-79554188	HMEC	breast:	n/a
15	chr7:79609099-79609149	IMR90	lung:	fetal
16	chr7:79554138-79554188	SKMC	muscle:	n/a
17	chr7:79554138-79554188	H1-hESC	embryonic stem cell:	embryo
18	chr7:79554138-79554188	MCF-7	breast:	n/a
19	chr7:79609099-79609149	MCF10A-Er-Src	breast:	n/a
20	chr7:79609099-79609149	A549	lung:	n/a
21	chr7:79554138-79554188	AG09319	gingival:	n/a
22	chr7:79554138-79554188	HIPEpiC	eye:	n/a
23	chr7:79554138-79554188	AG04449	skin:	fetal
24	chr7:79554138-79554188	HRPEpiC	eye:	n/a
25	chr7:79609099-79609149	GM12891	blood:	n/a
26	chr7:79609099-79609149	HNPCEpiC	eye:	n/a
27	chr7:79554138-79554188	GM12891	blood:	n/a
28	chr7:79554138-79554188	NHDF-neo	bronchial:	n/a
29	chr7:79554138-79554188	A549	lung:	n/a
30	chr7:79554138-79554188	PrEC	prostate:	n/a
31	chr7:79554138-79554188	BJ	skin:	n/a
32	chr7:79554138-79554188	CMK	blood:	n/a
33	chr7:79554138-79554188	HepG2	liver:	n/a
34	chr7:79609099-79609149	BE2_C	brain:	n/a
35	chr7:79554138-79554188	NT2-D1	testis:	n/a
36	chr7:79609099-79609149	SK-N-MC	brain:	n/a
37	chr7:79609099-79609149	HCT-116	colon:	n/a
38	chr7:79609099-79609149	RPTEC	kidney:	n/a
39	chr7:79609099-79609149	HEK293	kidney:	embryo
40	chr7:79554138-79554188	GM12892	blood:	n/a
41	chr7:79554138-79554188	HEEpiC	esophagus:	n/a
42	chr7:79609099-79609149	AG09309	skin:	n/a
43	chr7:79554138-79554188	ProgFib	skin:	n/a
44	chr7:79609099-79609149	T-47D	breast:	n/a
45	chr7:79609099-79609149	HCM	heart:	n/a
46	chr7:79554138-79554188	HCF	heart:	n/a
47	chr7:79554138-79554188	HEK293	kidney:	embryo
48	chr7:79609099-79609149	HRPEpiC	eye:	n/a
49	chr7:79554138-79554188	HPAEpiC	pulmonary alveolar:	n/a
50	chr7:79609099-79609149	AG04450	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr7:79522831..79524526-chr7:79524961..79527808,2	K562	blood:
2	chr7:79453655..79455461-chr7:79459874..79462573,2	K562	blood:
3	chr7:79435821..79436734-chr7:79648179..79648888,3	MCF-7	breast:
4	chr7:79453655..79455160-chr7:79459736..79461374,2	K562	blood:
5	chr7:79412469..79414428-chr7:79417950..79420307,2	K562	blood:
6	chr7:79453655..79455160-chr7:79459736..79461374,2	K562	blood:
7	chr3:193491807..193492652-chr7:79594775..79595639,2	MCF-7	breast:
8	chr7:79522831..79524526-chr7:79524961..79527808,2	K562	blood:
9	chr10:131908257..131908882-chr7:79551578..79552135,2	MCF-7	breast:
10	chr7:79453655..79455461-chr7:79459874..79462573,2	K562	blood:
11	chr7:79412469..79414428-chr7:79417950..79420307,2	K562	blood:

Variant related genes	Relation type
RNU6-849P	TF binding region
RNU6-849P	CpG island

Extended variants
information (count: 4332 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:4332 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10499847	chr7:79402551-79402552	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs114480344	chr7:79402553-79402554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs569426714	chr7:79402598-79402599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs557422685	chr7:79402613-79402614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs551876306	chr7:79402621-79402622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs374358997	chr7:79402652-79402653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs2714640	chr7:79402668-79402669	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs184805689	chr7:79402728-79402729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs147188669	chr7:79402759-79402760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs11979651	chr7:79402768-79402769	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs555382430	chr7:79402779-79402780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs140873684	chr7:79402835-79402836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs77388671	chr7:79402842-79402843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs116295507	chr7:79402850-79402851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs537672671	chr7:79402853-79402854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs557398023	chr7:79402862-79402863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs188022456	chr7:79402863-79402864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs539983963	chr7:79402867-79402868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs560093701	chr7:79402873-79402874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs148671652	chr7:79402892-79402893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs191331495	chr7:79402910-79402911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs142869085	chr7:79402913-79402914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs531905096	chr7:79402933-79402934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs551986636	chr7:79403028-79403029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs565506004	chr7:79403056-79403057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs184527368	chr7:79403060-79403061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs189797678	chr7:79403068-79403069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs181125539	chr7:79403076-79403077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs543191659	chr7:79403088-79403089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs151073276	chr7:79403129-79403130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs567608971	chr7:79403161-79403162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs576032533	chr7:79403180-79403181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs116006892	chr7:79403189-79403190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs113115138	chr7:79403204-79403205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs140994069	chr7:79403220-79403221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs568827312	chr7:79403224-79403225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs372851320	chr7:79403273-79403274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs546796746	chr7:79403334-79403335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs184893513	chr7:79403338-79403339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs557510705	chr7:79403340-79403341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs577465635	chr7:79403341-79403342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs558852151	chr7:79403343-79403344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs533879326	chr7:79403344-79403345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs553598220	chr7:79403371-79403372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs558644964	chr7:79403387-79403388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs112456026	chr7:79403404-79403405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs542272155	chr7:79403405-79403406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs571881578	chr7:79403427-79403428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs1851752	chr7:79403435-79403436	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs559657625	chr7:79403540-79403541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

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
Cancer	20164920	CNVD
Neurodevelopmental disorder	22521361	CNVD
Williams Syndrome	20824207	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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:477 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:79399400-79404800	Weak transcription	Fetal Lung	lung
2	chr7:79399400-79411000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr7:79404800-79405800	Enhancers	Fetal Lung	lung
4	chr7:79405800-79406600	Weak transcription	Fetal Lung	lung
5	chr7:79407000-79407800	Enhancers	Monocytes-CD14+_RO01746	blood
6	chr7:79407200-79407600	Enhancers	Fetal Heart	heart
7	chr7:79407200-79408200	Enhancers	Muscle Satellite Cultured Cells	--
8	chr7:79407200-79408600	Enhancers	Primary monocytes fromperipheralblood	blood
9	chr7:79407600-79408200	Enhancers	Osteobl	bone
10	chr7:79407600-79408400	Enhancers	HMEC	breast
11	chr7:79407600-79410800	Weak transcription	Fetal Heart	heart
12	chr7:79407800-79408000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr7:79407800-79408400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr7:79407800-79408600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
15	chr7:79407800-79408800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr7:79407800-79409000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr7:79407800-79409000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr7:79407800-79409000	Enhancers	NHLF	lung
19	chr7:79408000-79408400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr7:79408000-79408600	Enhancers	Primary neutrophils fromperipheralblood	blood
21	chr7:79408000-79409000	Enhancers	NH-A	brain
22	chr7:79408000-79409200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr7:79408200-79408400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
24	chr7:79408200-79408400	Enhancers	NHDF-Ad	bronchial
25	chr7:79408200-79408600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr7:79408200-79409000	Flanking Active TSS	Osteobl	bone
27	chr7:79408400-79408600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr7:79408400-79408600	Enhancers	Muscle Satellite Cultured Cells	--
29	chr7:79408400-79408800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr7:79408400-79408800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr7:79408400-79408800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr7:79408400-79408800	Enhancers	Adipose Nuclei	Adipose
33	chr7:79408400-79408800	Active TSS	Hela-S3	cervix
34	chr7:79408400-79408800	Flanking Active TSS	HMEC	breast
35	chr7:79408400-79409000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr7:79408600-79408800	Flanking Active TSS	Muscle Satellite Cultured Cells	--
37	chr7:79408600-79408800	Active TSS	Monocytes-CD14+_RO01746	blood
38	chr7:79408600-79409000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr7:79408600-79409000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
40	chr7:79408600-79409000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr7:79408600-79409200	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
42	chr7:79408800-79409000	Enhancers	Muscle Satellite Cultured Cells	--
43	chr7:79408800-79409000	Enhancers	HMEC	breast
44	chr7:79408800-79409000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
45	chr7:79408800-79409200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr7:79409000-79409200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr7:79409000-79409200	Enhancers	Primary neutrophils fromperipheralblood	blood
48	chr7:79409000-79409200	Active TSS	Monocytes-CD14+_RO01746	blood
49	chr7:79409000-79409200	Enhancers	Osteobl	bone
50	chr7:79409000-79410400	Weak transcription	Fetal Lung	lung

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