Variant report

Variant	nsv538746
Chromosome Location	chr7:15368522-15554763
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:547)
CpG islands
(count:183)
Chromatin interactive
region (count:7)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:547 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

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	ATF1	chr7:15447516-15447947	K562	blood:	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	BRCA1	chr7:15511560-15511688	Hela-S3	cervix:	n/a	n/a
6	CCNT2	chr7:15392105-15392305	K562	blood:	n/a	chr7:15392156-15392165
7	CEBPB	chr7:15374237-15374521	A549	lung:	n/a	n/a
8	CEBPB	chr7:15405775-15405910	HepG2	liver:	n/a	n/a
9	CEBPB	chr7:15506113-15506415	IMR90	lung:	n/a	chr7:15506286-15506297
10	CEBPB	chr7:15466850-15467116	HepG2	liver:	n/a	chr7:15466942-15466953
11	CEBPB	chr7:15405781-15406007	HepG2	liver:	n/a	n/a
12	CEBPB	chr7:15377052-15377067	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr7:15435469-15435633	K562	blood:	n/a	n/a
14	CEBPB	chr7:15478370-15478666	IMR90	lung:	n/a	chr7:15478519-15478530
15	CEBPB	chr7:15544100-15544369	A549	lung:	n/a	chr7:15544193-15544204
16	CEBPB	chr7:15415765-15415909	HepG2	liver:	n/a	n/a
17	CEBPB	chr7:15478389-15478692	HepG2	liver:	n/a	chr7:15478519-15478530
18	CEBPB	chr7:15458749-15459010	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr7:15506112-15506438	HepG2	liver:	n/a	chr7:15506286-15506297
20	CEBPB	chr7:15374252-15374552	HepG2	liver:	n/a	n/a
21	CEBPB	chr7:15468127-15468377	HepG2	liver:	n/a	chr7:15468226-15468237
22	CEBPB	chr7:15435411-15435690	HepG2	liver:	n/a	n/a
23	CEBPB	chr7:15506122-15506411	A549	lung:	n/a	chr7:15506286-15506297
24	CEBPB	chr7:15426024-15426286	HepG2	liver:	n/a	chr7:15426145-15426154 chr7:15426143-15426154
25	CEBPB	chr7:15483624-15483679	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr7:15483484-15483779	IMR90	lung:	n/a	chr7:15483605-15483616
27	CEBPB	chr7:15468148-15468383	IMR90	lung:	n/a	chr7:15468226-15468237
28	CEBPB	chr7:15478355-15478692	A549	lung:	n/a	chr7:15478519-15478530
29	CEBPB	chr7:15447539-15447839	K562	blood:	n/a	n/a
30	CEBPB	chr7:15466810-15467126	IMR90	lung:	n/a	chr7:15466942-15466953
31	CEBPB	chr7:15466804-15467001	K562	blood:	n/a	chr7:15466942-15466953
32	CEBPB	chr7:15447580-15447867	HepG2	liver:	n/a	n/a
33	CEBPB	chr7:15458723-15459054	HepG2	liver:	n/a	n/a
34	CEBPB	chr7:15408089-15408100	K562	blood:	n/a	n/a
35	CEBPB	chr7:15483579-15483676	K562	blood:	n/a	chr7:15483605-15483616
36	CEBPB	chr7:15515554-15515644	A549	lung:	n/a	n/a
37	CEBPB	chr7:15483429-15483757	HepG2	liver:	n/a	chr7:15483605-15483616
38	CEBPB	chr7:15374309-15374579	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr7:15435437-15435631	A549	lung:	n/a	n/a
40	CEBPB	chr7:15458726-15459040	A549	lung:	n/a	n/a
41	CEBPB	chr7:15458696-15459049	IMR90	lung:	n/a	n/a
42	CTCF	chr7:15428820-15428970	MCF-7	breast:	n/a	n/a
43	CTCF	chr7:15543620-15543770	NHDF-neo	bronchial:	n/a	chr7:15543671-15543679 chr7:15543711-15543727
44	CTCF	chr7:15543660-15543810	HBMEC	blood vessel:	n/a	chr7:15543671-15543679 chr7:15543711-15543727
45	CTCF	chr7:15428820-15428970	GM12874	blood:	n/a	n/a
46	CTCF	chr7:15428844-15428968	MCF-7	breast:	n/a	n/a
47	CTCF	chr7:15543680-15543830	AG04449	skin:	n/a	chr7:15543711-15543727
48	CTCF	chr7:15428800-15428950	AG09319	gingival:	n/a	n/a
49	CTCF	chr7:15409109-15409208	Medullo	brain:	n/a	n/a
50	CTCF	chr7:15543576-15543829	IMR90	lung:	n/a	chr7:15543671-15543679 chr7:15543711-15543727

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:15392612-15392662	NHBE	bronchial:	n/a
2	chr7:15436238-15436288	GM19239	blood:	n/a
3	chr7:15392612-15392662	GM06990	blood:	n/a
4	chr7:15392612-15392662	GM19239	blood:	n/a
5	chr7:15392612-15392662	HNPCEpiC	eye:	n/a
6	chr7:15436238-15436288	ECC-1	luminal epithelium:	n/a
7	chr7:15392612-15392662	SK-N-SH	brain:	n/a
8	chr7:15436848-15436898	GM12892	blood:	n/a
9	chr7:15392612-15392662	U87	brain:	n/a
10	chr7:15436238-15436288	GM06990	blood:	n/a
11	chr7:15392612-15392662	GM12892	blood:	n/a
12	chr7:15392612-15392662	ECC-1	luminal epithelium:	n/a
13	chr7:15436848-15436898	PANC-1	pancreas:	n/a
14	chr7:15392612-15392662	AG04449	skin:	fetal
15	chr7:15436848-15436898	NHBE	bronchial:	n/a
16	chr7:15436238-15436288	NT2-D1	testis:	n/a
17	chr7:15436848-15436898	HRPEpiC	eye:	n/a
18	chr7:15436848-15436898	HepG2	liver:	n/a
19	chr7:15436238-15436288	AG04450	lung:	fetal
20	chr7:15392612-15392662	Hela-S3	cervix:	n/a
21	chr7:15436238-15436288	HL-60	blood:	n/a
22	chr7:15436848-15436898	GM06990	blood:	n/a
23	chr7:15436848-15436898	SK-N-SH	brain:	n/a
24	chr7:15436238-15436288	HPAEpiC	pulmonary alveolar:	n/a
25	chr7:15436848-15436898	RPTEC	kidney:	n/a
26	chr7:15436238-15436288	HNPCEpiC	eye:	n/a
27	chr7:15436238-15436288	HepG2	liver:	n/a
28	chr7:15436848-15436898	BE2_C	brain:	n/a
29	chr7:15436848-15436898	MCF10A-Er-Src	breast:	n/a
30	chr7:15436238-15436288	HRPEpiC	eye:	n/a
31	chr7:15392612-15392662	HRE	kidney:	n/a
32	chr7:15436848-15436898	NB4	blood:	n/a
33	chr7:15392612-15392662	PANC-1	pancreas:	n/a
34	chr7:15436238-15436288	SK-N-SH_RA	brain:	n/a
35	chr7:15392612-15392662	PFSK-1	brain:	n/a
36	chr7:15392612-15392662	GM12878	blood:	n/a
37	chr7:15436238-15436288	AG09309	skin:	n/a
38	chr7:15436238-15436288	SAEC	small airway:	n/a
39	chr7:15436238-15436288	RPTEC	kidney:	n/a
40	chr7:15436238-15436288	BJ	skin:	n/a
41	chr7:15436848-15436898	HCM	heart:	n/a
42	chr7:15436848-15436898	HMEC	breast:	n/a
43	chr7:15436848-15436898	Caco-2	colon:	n/a
44	chr7:15436848-15436898	SK-N-MC	brain:	n/a
45	chr7:15392612-15392662	HEK293	kidney:	embryo
46	chr7:15436848-15436898	AG10803	skin:	n/a
47	chr7:15436238-15436288	HRE	kidney:	n/a
48	chr7:15392612-15392662	AG04450	lung:	fetal
49	chr7:15436848-15436898	BJ	skin:	n/a
50	chr7:15392612-15392662	NHDF-neo	bronchial:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:15543347..15544306-chr7:15760242..15761135,3	MCF-7	breast:
2	chr7:15531844..15534427-chr7:15538603..15541203,2	K562	blood:
3	chr7:15392439..15394759-chr7:15395448..15398263,2	K562	blood:
4	chr7:15392439..15394759-chr7:15395448..15398263,2	K562	blood:
5	chr7:15531844..15534427-chr7:15538603..15541203,2	K562	blood:
6	chr7:15422858..15425258-chr7:15428818..15431707,2	K562	blood:
7	chr7:15422858..15425258-chr7:15428818..15431707,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MEOX2-6	chr7:15433738-15433804	NONHSAT119276
2	lnc-MEOX2-5	chr7:15494576-15494813	NONHSAT119277
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: 8957 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:8957 , 50 per page) page: 1 2 3 4 5 6 7 ... 180

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs574916333	chr7:15368522-15368523	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs150076895	chr7:15368528-15368529	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs563648573	chr7:15368557-15368558	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs182085681	chr7:15368582-15368583	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs552505157	chr7:15368598-15368599	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs564740931	chr7:15368619-15368620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs117995195	chr7:15368655-15368656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs546915101	chr7:15368659-15368660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs565319346	chr7:15368670-15368671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs535857668	chr7:15368708-15368709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs186724559	chr7:15368720-15368721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs62450333	chr7:15368729-15368730	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs569657093	chr7:15368732-15368733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs191134109	chr7:15368735-15368736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs558465150	chr7:15368741-15368742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs570675370	chr7:15368759-15368760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs371344641	chr7:15368778-15368779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs534893975	chr7:15368787-15368788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs553339010	chr7:15368788-15368789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs138376093	chr7:15368798-15368799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs542266435	chr7:15368815-15368816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs557384523	chr7:15368831-15368832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs374651857	chr7:15368852-15368853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs141687142	chr7:15368872-15368873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs145322835	chr7:15368880-15368881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs117106796	chr7:15368911-15368912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs573406886	chr7:15368930-15368931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs138061505	chr7:15368956-15368957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs562063538	chr7:15368979-15368980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs529593742	chr7:15368982-15368983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs142523052	chr7:15368989-15368990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs73064524	chr7:15369035-15369036	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs530519814	chr7:15369061-15369062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs182917795	chr7:15369076-15369077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs570646025	chr7:15369077-15369078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs115150209	chr7:15369084-15369085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs553277347	chr7:15369097-15369098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs77107255	chr7:15369100-15369101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs10216324	chr7:15369119-15369120	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs375818483	chr7:15369122-15369123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs78227847	chr7:15369153-15369154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs115167946	chr7:15369207-15369208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs148262969	chr7:15369235-15369236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs369870633	chr7:15369262-15369263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs373064367	chr7:15369278-15369279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs188423758	chr7:15369303-15369304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs558245642	chr7:15369349-15369350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs192896434	chr7:15369378-15369379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs185297514	chr7:15369402-15369403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs187725860	chr7:15369441-15369442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

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
Osteosarcoma	21215367	CNVD
Bladder cancer	21909424	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:433 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:15363800-15370400	Weak transcription	NHDF-Ad	bronchial
2	chr7:15367800-15378600	Weak transcription	Liver	Liver
3	chr7:15368200-15368600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr7:15368600-15370600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr7:15370400-15370800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr7:15370400-15370800	Enhancers	NHDF-Ad	bronchial
7	chr7:15370400-15371000	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr7:15370400-15371000	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr7:15370400-15371000	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr7:15370400-15371200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr7:15370600-15370800	Enhancers	H9 Cell Line	embryonic stem cell
12	chr7:15370600-15370800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr7:15370600-15371000	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr7:15370600-15371000	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr7:15370600-15371000	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr7:15370800-15371000	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr7:15370800-15374200	Weak transcription	H9 Cell Line	embryonic stem cell
18	chr7:15371000-15371800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr7:15371000-15372600	Weak transcription	HUES48 Cell Line	embryonic stem cell
20	chr7:15371000-15372600	Weak transcription	HUES64 Cell Line	embryonic stem cell
21	chr7:15371000-15372600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
22	chr7:15371000-15372600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
23	chr7:15371000-15373400	Weak transcription	HUES6 Cell Line	embryonic stem cell
24	chr7:15371800-15374600	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr7:15372000-15372400	Enhancers	H1 Cell Line	embryonic stem cell
26	chr7:15372400-15372800	Weak transcription	H1 Cell Line	embryonic stem cell
27	chr7:15372600-15372800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr7:15372600-15373200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
29	chr7:15372600-15374600	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr7:15372600-15374800	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr7:15372600-15374800	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr7:15372600-15375000	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr7:15372600-15375000	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr7:15372800-15373000	Enhancers	H1 Cell Line	embryonic stem cell
35	chr7:15372800-15373000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr7:15373000-15374200	Weak transcription	H1 Cell Line	embryonic stem cell
37	chr7:15373400-15374600	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr7:15374000-15374800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
39	chr7:15374200-15374600	Enhancers	H1 Cell Line	embryonic stem cell
40	chr7:15374200-15374600	Enhancers	H9 Cell Line	embryonic stem cell
41	chr7:15374400-15375400	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr7:15375200-15375400	Enhancers	Fetal Muscle Leg	muscle
43	chr7:15375600-15376400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr7:15376200-15376800	Weak transcription	Fetal Muscle Leg	muscle
45	chr7:15377000-15377400	Enhancers	Fetal Muscle Leg	muscle
46	chr7:15377200-15377400	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr7:15378600-15379000	ZNF genes & repeats	Liver	Liver
48	chr7:15379000-15380000	Weak transcription	Liver	Liver
49	chr7:15380000-15380800	ZNF genes & repeats	Liver	Liver
50	chr7:15380400-15380800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin

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