Variant report

Variant	nsv1033428
Chromosome Location	chr7:15343210-15554763
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:973)
CpG islands
(count:183)
Chromatin interactive
region (count:18)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:973 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:15416281-15416587	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:15365751-15365978	HepG2	liver:	n/a	n/a
3	ATF1	chr7:15396881-15397102	K562	blood:	n/a	n/a
4	ATF1	chr7:15392479-15392850	K562	blood:	n/a	n/a
5	ATF1	chr7:15447516-15447947	K562	blood:	n/a	n/a
6	ATF1	chr7:15365824-15366012	K562	blood:	n/a	n/a
7	BACH1	chr7:15365724-15365854	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr7:15344096-15344290	GM12878	blood:	n/a	chr7:15344230-15344240 chr7:15344229-15344240
9	BRCA1	chr7:15358586-15358654	Hela-S3	cervix:	n/a	n/a
10	BRCA1	chr7:15511560-15511688	Hela-S3	cervix:	n/a	n/a
11	CCNT2	chr7:15354406-15354606	K562	blood:	n/a	n/a
12	CCNT2	chr7:15392105-15392305	K562	blood:	n/a	chr7:15392156-15392165
13	CEBPB	chr7:15447539-15447839	K562	blood:	n/a	n/a
14	CEBPB	chr7:15415765-15415909	HepG2	liver:	n/a	n/a
15	CEBPB	chr7:15348292-15348648	HepG2	liver:	n/a	n/a
16	CEBPB	chr7:15483579-15483676	K562	blood:	n/a	chr7:15483605-15483616
17	CEBPB	chr7:15364285-15364576	HepG2	liver:	n/a	chr7:15364403-15364414
18	CEBPB	chr7:15359298-15359308	A549	lung:	n/a	n/a
19	CEBPB	chr7:15435411-15435690	HepG2	liver:	n/a	n/a
20	CEBPB	chr7:15374252-15374552	HepG2	liver:	n/a	n/a
21	CEBPB	chr7:15374237-15374521	A549	lung:	n/a	n/a
22	CEBPB	chr7:15405781-15406007	HepG2	liver:	n/a	n/a
23	CEBPB	chr7:15435437-15435631	A549	lung:	n/a	n/a
24	CEBPB	chr7:15364258-15364551	A549	lung:	n/a	chr7:15364403-15364414
25	CEBPB	chr7:15408089-15408100	K562	blood:	n/a	n/a
26	CEBPB	chr7:15363413-15363459	IMR90	lung:	n/a	chr7:15363437-15363448
27	CEBPB	chr7:15458726-15459040	A549	lung:	n/a	n/a
28	CEBPB	chr7:15364236-15364515	IMR90	lung:	n/a	chr7:15364403-15364414
29	CEBPB	chr7:15478389-15478692	HepG2	liver:	n/a	chr7:15478519-15478530
30	CEBPB	chr7:15483484-15483779	IMR90	lung:	n/a	chr7:15483605-15483616
31	CEBPB	chr7:15478355-15478692	A549	lung:	n/a	chr7:15478519-15478530
32	CEBPB	chr7:15478370-15478666	IMR90	lung:	n/a	chr7:15478519-15478530
33	CEBPB	chr7:15468148-15468383	IMR90	lung:	n/a	chr7:15468226-15468237
34	CEBPB	chr7:15458696-15459049	IMR90	lung:	n/a	n/a
35	CEBPB	chr7:15506113-15506415	IMR90	lung:	n/a	chr7:15506286-15506297
36	CEBPB	chr7:15483429-15483757	HepG2	liver:	n/a	chr7:15483605-15483616
37	CEBPB	chr7:15426024-15426286	HepG2	liver:	n/a	chr7:15426145-15426154 chr7:15426143-15426154
38	CEBPB	chr7:15458749-15459010	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr7:15374309-15374579	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr7:15348308-15348628	A549	lung:	n/a	n/a
41	CEBPB	chr7:15348291-15348635	IMR90	lung:	n/a	n/a
42	CEBPB	chr7:15364360-15364438	H1-hESC	embryonic stem cell:	n/a	chr7:15364403-15364414
43	CEBPB	chr7:15468127-15468377	HepG2	liver:	n/a	chr7:15468226-15468237
44	CEBPB	chr7:15544100-15544369	A549	lung:	n/a	chr7:15544193-15544204
45	CEBPB	chr7:15466850-15467116	HepG2	liver:	n/a	chr7:15466942-15466953
46	CEBPB	chr7:15377052-15377067	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr7:15506122-15506411	A549	lung:	n/a	chr7:15506286-15506297
48	CEBPB	chr7:15435469-15435633	K562	blood:	n/a	n/a
49	CEBPB	chr7:15515554-15515644	A549	lung:	n/a	n/a
50	CEBPB	chr7:15363362-15363478	A549	lung:	n/a	chr7:15363437-15363448

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:15436238-15436288	AoSMC	blood vessel:	n/a
2	chr7:15436848-15436898	HEK293	kidney:	embryo
3	chr7:15436238-15436288	MCF10A-Er-Src	breast:	n/a
4	chr7:15392612-15392662	LNCaP	prostate:	n/a
5	chr7:15436848-15436898	GM12892	blood:	n/a
6	chr7:15436238-15436288	HCF	heart:	n/a
7	chr7:15436238-15436288	HRE	kidney:	n/a
8	chr7:15436238-15436288	U87	brain:	n/a
9	chr7:15436848-15436898	GM12878	blood:	n/a
10	chr7:15436848-15436898	SKMC	muscle:	n/a
11	chr7:15392612-15392662	ECC-1	luminal epithelium:	n/a
12	chr7:15392612-15392662	AG10803	skin:	n/a
13	chr7:15436848-15436898	HCF	heart:	n/a
14	chr7:15436238-15436288	A549	lung:	n/a
15	chr7:15436238-15436288	HepG2	liver:	n/a
16	chr7:15436238-15436288	GM12891	blood:	n/a
17	chr7:15392612-15392662	MCF10A-Er-Src	breast:	n/a
18	chr7:15392612-15392662	GM19239	blood:	n/a
19	chr7:15392612-15392662	HCM	heart:	n/a
20	chr7:15392612-15392662	HPAEpiC	pulmonary alveolar:	n/a
21	chr7:15436238-15436288	HRCEpiC	kidney:	n/a
22	chr7:15436848-15436898	AoSMC	blood vessel:	n/a
23	chr7:15436848-15436898	U87	brain:	n/a
24	chr7:15392612-15392662	SAEC	small airway:	n/a
25	chr7:15392612-15392662	Hela-S3	cervix:	n/a
26	chr7:15436238-15436288	SK-N-SH	brain:	n/a
27	chr7:15436238-15436288	HAEpiC	amniotic membrane:	n/a
28	chr7:15392612-15392662	PrEC	prostate:	n/a
29	chr7:15436848-15436898	BE2_C	brain:	n/a
30	chr7:15392612-15392662	BJ	skin:	n/a
31	chr7:15436848-15436898	GM19239	blood:	n/a
32	chr7:15436848-15436898	A549	lung:	n/a
33	chr7:15392612-15392662	K562	blood:	n/a
34	chr7:15392612-15392662	IMR90	lung:	fetal
35	chr7:15436238-15436288	AG10803	skin:	n/a
36	chr7:15392612-15392662	GM06990	blood:	n/a
37	chr7:15392612-15392662	GM12891	blood:	n/a
38	chr7:15436238-15436288	T-47D	breast:	n/a
39	chr7:15436238-15436288	HIPEpiC	eye:	n/a
40	chr7:15392612-15392662	HepG2	liver:	n/a
41	chr7:15436848-15436898	NB4	blood:	n/a
42	chr7:15436238-15436288	NT2-D1	testis:	n/a
43	chr7:15392612-15392662	Caco-2	colon:	n/a
44	chr7:15392612-15392662	BE2_C	brain:	n/a
45	chr7:15392612-15392662	HNPCEpiC	eye:	n/a
46	chr7:15436238-15436288	PFSK-1	brain:	n/a
47	chr7:15436238-15436288	ProgFib	skin:	n/a
48	chr7:15436848-15436898	H1-hESC	embryonic stem cell:	embryo
49	chr7:15392612-15392662	HAEpiC	amniotic membrane:	n/a
50	chr7:15436238-15436288	PANC-1	pancreas:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:15344409..15345014-chr7:16111015..16111547,2	MCF-7	breast:
2	chr7:15344369..15345259-chr7:16109147..16109752,2	MCF-7	breast:
3	chr7:15543347..15544306-chr7:15760242..15761135,3	MCF-7	breast:
4	chr7:14757340..14758014-chr7:15344576..15345303,4	MCF-7	breast:
5	chr7:15422858..15425258-chr7:15428818..15431707,2	K562	blood:
6	chr7:15365434..15366404-chr7:16110606..16111525,6	MCF-7	breast:
7	chr7:15365462..15366327-chr7:15594881..15595525,2	MCF-7	breast:
8	chr7:15364860..15366538-chr7:15760053..15761291,7	MCF-7	breast:
9	chr7:15392439..15394759-chr7:15395448..15398263,2	K562	blood:
10	chr7:15344411..15345401-chr7:15760276..15761708,4	MCF-7	breast:
11	chr7:15531844..15534427-chr7:15538603..15541203,2	K562	blood:
12	chr7:15392439..15394759-chr7:15395448..15398263,2	K562	blood:
13	chr7:15365379..15366315-chr7:15760483..15761223,4	MCF-7	breast:
14	chr7:15422858..15425258-chr7:15428818..15431707,2	K562	blood:
15	chr7:15344361..15344992-chr7:15760353..15761140,2	MCF-7	breast:
16	chr7:15365402..15367803-chr7:15593636..15595869,2	MCF-7	breast:
17	chr7:15365412..15365978-chr7:15759570..15760468,2	MCF-7	breast:
18	chr7:15531844..15534427-chr7:15538603..15541203,2	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MEOX2-5	chr7:15494576-15494813	NONHSAT119277
2	lnc-MEOX2-6	chr7:15433738-15433804	NONHSAT119276
3	lnc-MEOX2-6	chr7:15435671-15436219	NONHSAT119276

No data

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

Extended variants
information (count: 9847 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:9847 , 50 per page) page: 1 2 3 4 5 6 7 ... 197

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs182897951	chr7:15343216-15343217	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs568366118	chr7:15343233-15343234	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs77881767	chr7:15343273-15343274	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs4439006	chr7:15343306-15343307	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs73062585	chr7:15343318-15343319	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs540018093	chr7:15343329-15343330	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs558091830	chr7:15343347-15343348	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs377367450	chr7:15343374-15343375	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs140816262	chr7:15343386-15343387	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs188402861	chr7:15343392-15343393	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs73284560	chr7:15343410-15343411	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs574082135	chr7:15343423-15343424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs565677895	chr7:15343426-15343427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs541457436	chr7:15343452-15343453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs563020801	chr7:15343481-15343482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs530540213	chr7:15343500-15343501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs370497805	chr7:15343569-15343570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs563485940	chr7:15343579-15343580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs145514351	chr7:15343611-15343612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs148862472	chr7:15343615-15343616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs143493466	chr7:15343642-15343643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs530995390	chr7:15343682-15343683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs529290370	chr7:15343694-15343695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs112212076	chr7:15343698-15343699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs73284561	chr7:15343724-15343725	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs539567101	chr7:15343730-15343731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs558292593	chr7:15343743-15343744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs192130808	chr7:15343772-15343773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs184723064	chr7:15343796-15343797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs187709157	chr7:15343830-15343831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs192556471	chr7:15343856-15343857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs543722850	chr7:15343860-15343861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs183678858	chr7:15343873-15343874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs556552705	chr7:15343879-15343880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs377085753	chr7:15343892-15343893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs552680583	chr7:15343915-15343916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs189077479	chr7:15343924-15343925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs572942606	chr7:15343980-15343981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs557404871	chr7:15343982-15343983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs181021383	chr7:15343994-15343995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs562269754	chr7:15344006-15344007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs373024797	chr7:15344019-15344020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs11768557	chr7:15344117-15344118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs561942182	chr7:15344138-15344139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs529227386	chr7:15344146-15344147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs140818023	chr7:15344177-15344178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs371078720	chr7:15344181-15344182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs562882258	chr7:15344190-15344191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs10244911	chr7:15344230-15344231	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs551571500	chr7:15344237-15344238	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Melanoma	17363583	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21858162	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Rubinstein-Taybi syndrome	22470819	CNVD
Alzheimer''s disease	22166940	CNVD
Abnormal phenotypes	18644119	CNVD
Non-syndromic sensorineural hearing loss	22570644	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Osteosarcoma	21215367	CNVD
Bladder cancer	21909424	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:487 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:15337200-15346800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr7:15342400-15343400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr7:15343000-15343400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr7:15344200-15344600	Enhancers	NHDF-Ad	bronchial
5	chr7:15344400-15345000	Enhancers	Liver	Liver
6	chr7:15344600-15345000	Weak transcription	NHDF-Ad	bronchial
7	chr7:15345000-15345200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr7:15345000-15345200	Enhancers	NHDF-Ad	bronchial
9	chr7:15345200-15349400	Weak transcription	NHDF-Ad	bronchial
10	chr7:15345200-15352800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr7:15346800-15347000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr7:15347000-15347600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr7:15347400-15347800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr7:15347600-15347800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr7:15348600-15348800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr7:15348600-15348800	Enhancers	Fetal Muscle Leg	muscle
17	chr7:15349400-15349600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr7:15349400-15350000	Enhancers	Fetal Brain Male	brain
19	chr7:15349400-15350600	Enhancers	NHDF-Ad	bronchial
20	chr7:15349600-15349800	Enhancers	Fetal Muscle Leg	muscle
21	chr7:15350000-15350400	Weak transcription	Fetal Brain Male	brain
22	chr7:15350400-15350800	Enhancers	Fetal Brain Male	brain
23	chr7:15352400-15353200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr7:15352800-15353600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr7:15353000-15353800	Enhancers	Liver	Liver
26	chr7:15355800-15356200	Enhancers	Fetal Intestine Small	intestine
27	chr7:15355800-15356600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr7:15355800-15357200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr7:15360600-15361400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr7:15361000-15361400	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr7:15363000-15363600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr7:15363200-15363800	Enhancers	Osteobl	bone
33	chr7:15363400-15363600	Active TSS	Fetal Lung	lung
34	chr7:15363400-15363800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr7:15363400-15363800	Enhancers	NHDF-Ad	bronchial
36	chr7:15363400-15364000	Enhancers	Liver	Liver
37	chr7:15363400-15364000	Enhancers	Brain Inferior Temporal Lobe	brain
38	chr7:15363400-15364000	Enhancers	Brain Substantia Nigra	brain
39	chr7:15363600-15363800	Flanking Active TSS	Fetal Lung	lung
40	chr7:15363800-15364000	Enhancers	Fetal Lung	lung
41	chr7:15363800-15365200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr7:15363800-15370400	Weak transcription	NHDF-Ad	bronchial
43	chr7:15364000-15365800	Weak transcription	Fetal Lung	lung
44	chr7:15364000-15366000	Weak transcription	Liver	Liver
45	chr7:15364000-15366000	Weak transcription	Brain Inferior Temporal Lobe	brain
46	chr7:15364400-15364600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr7:15365200-15365400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr7:15365400-15365800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr7:15365800-15366200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr7:15365800-15366200	Enhancers	Fetal Lung	lung

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