Variant report

Variant	nsv606279
Chromosome Location	chr7:13995209-14027991
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:414)
CpG islands
(count:61)
Chromatin interactive
region (count:44)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:414 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:14025489-14026374	K562	blood:	n/a	n/a
2	ARID3A	chr7:14022012-14023126	K562	blood:	n/a	n/a
3	ARID3A	chr7:14023492-14023912	K562	blood:	n/a	n/a
4	ARID3A	chr7:14019807-14021691	K562	blood:	n/a	chr7:14020786-14020802 chr7:14020787-14020803
5	ARID3A	chr7:14027058-14028051	K562	blood:	n/a	n/a
6	ARID3A	chr7:14024325-14025263	K562	blood:	n/a	n/a
7	ATF1	chr7:14019904-14020081	K562	blood:	n/a	n/a
8	ATF1	chr7:14022540-14022952	K562	blood:	n/a	n/a
9	ATF1	chr7:14027694-14028014	K562	blood:	n/a	n/a
10	ATF1	chr7:14027157-14027465	K562	blood:	n/a	n/a
11	ATF1	chr7:14020698-14021136	K562	blood:	n/a	n/a
12	ATF3	chr7:14022508-14022915	K562	blood:	n/a	n/a
13	ATF3	chr7:14020788-14020993	K562	blood:	n/a	n/a
14	ATF3	chr7:14020590-14021036	K562	blood:	n/a	n/a
15	BACH1	chr7:14020708-14021014	H1-hESC	embryonic stem cell:	n/a	chr7:14020850-14020864
16	BCLAF1	chr7:14020709-14021202	K562	blood:	n/a	chr7:14020853-14020862 chr7:14020852-14020861
17	BHLHE40	chr7:14027538-14032370	K562	blood:	n/a	n/a
18	BHLHE40	chr7:14020621-14021121	K562	blood:	n/a	n/a
19	CBX3	chr7:14020686-14021294	HCT-116	colon:	n/a	n/a
20	CCNT2	chr7:14020845-14021045	K562	blood:	n/a	n/a
21	CCNT2	chr7:14025553-14025753	K562	blood:	n/a	n/a
22	CCNT2	chr7:14027613-14027934	K562	blood:	n/a	n/a
23	CCNT2	chr7:14019439-14019595	K562	blood:	n/a	n/a
24	CCNT2	chr7:14022390-14022906	K562	blood:	n/a	n/a
25	CEBPB	chr7:14024708-14025085	K562	blood:	n/a	chr7:14024803-14024814 chr7:14024883-14024894
26	CEBPB	chr7:14020654-14021116	K562	blood:	n/a	n/a
27	CEBPB	chr7:14024748-14024990	HepG2	liver:	n/a	chr7:14024803-14024814 chr7:14024883-14024894
28	CEBPB	chr7:14020713-14021145	IMR90	lung:	n/a	n/a
29	CEBPB	chr7:14025392-14025544	H1-hESC	embryonic stem cell:	n/a	chr7:14025468-14025481
30	CEBPB	chr7:14019316-14020073	IMR90	lung:	n/a	chr7:14019938-14019949
31	CEBPB	chr7:14024785-14025050	IMR90	lung:	n/a	chr7:14024803-14024814 chr7:14024883-14024894
32	CEBPB	chr7:14022555-14022766	K562	blood:	n/a	n/a
33	CEBPB	chr7:14019756-14020094	K562	blood:	n/a	chr7:14019938-14019949
34	CEBPB	chr7:14024790-14024990	A549	lung:	n/a	chr7:14024803-14024814 chr7:14024883-14024894
35	CEBPB	chr7:14020519-14021361	HCT-116	colon:	n/a	n/a
36	CEBPB	chr7:14022307-14022889	K562	blood:	n/a	n/a
37	CEBPB	chr7:14017975-14018315	IMR90	lung:	n/a	n/a
38	CEBPB	chr7:14026370-14026599	K562	blood:	n/a	n/a
39	CEBPB	chr7:14022272-14022907	K562	blood:	n/a	n/a
40	CEBPB	chr7:14018578-14018927	K562	blood:	n/a	n/a
41	CEBPB	chr7:14020633-14021062	K562	blood:	n/a	n/a
42	CHD1	chr7:14027612-14030923	H1-hESC	embryonic stem cell:	n/a	chr7:14030234-14030244
43	CHD2	chr7:14015889-14016052	K562	blood:	n/a	n/a
44	CHD2	chr7:14027811-14027861	K562	blood:	n/a	n/a
45	CREB1	chr7:14026975-14027526	K562	blood:	n/a	n/a
46	CTCF	chr7:14026653-14026769	K562	blood:	n/a	n/a
47	CTCF	chr7:14014187-14014190	GM10266	blood:	n/a	n/a
48	CTCF	chr7:14014480-14014630	GM12868	blood:	n/a	n/a
49	CTCF	chr7:14027940-14028090	HPAF	blood vessel:	n/a	n/a
50	CTCF	chr7:14022215-14022355	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:14025907-14025957	HL-60	blood:	n/a
2	chr7:14025907-14025957	PFSK-1	brain:	n/a
3	chr7:14025907-14025957	GM19239	blood:	n/a
4	chr7:14025907-14025957	HNPCEpiC	eye:	n/a
5	chr7:14025907-14025957	CMK	blood:	n/a
6	chr7:14025907-14025957	SK-N-SH	brain:	n/a
7	chr7:14025907-14025957	HEK293	kidney:	embryo
8	chr7:14025907-14025957	NHDF-neo	bronchial:	n/a
9	chr7:14025907-14025957	Jurkat	blood:	n/a
10	chr7:14025907-14025957	GM12892	blood:	n/a
11	chr7:14025907-14025957	AG04450	lung:	fetal
12	chr7:14025907-14025957	NT2-D1	testis:	n/a
13	chr7:14025907-14025957	AG09309	skin:	n/a
14	chr7:14025907-14025957	HEEpiC	esophagus:	n/a
15	chr7:14025907-14025957	SAEC	small airway:	n/a
16	chr7:14025907-14025957	PrEC	prostate:	n/a
17	chr7:14025907-14025957	GM12878	blood:	n/a
18	chr7:14025907-14025957	AG09319	gingival:	n/a
19	chr7:14025907-14025957	ProgFib	skin:	n/a
20	chr7:14025907-14025957	HRCEpiC	kidney:	n/a
21	chr7:14025907-14025957	AG04449	skin:	fetal
22	chr7:14025907-14025957	HMEC	breast:	n/a
23	chr7:14025907-14025957	HRE	kidney:	n/a
24	chr7:14025907-14025957	SK-N-MC	brain:	n/a
25	chr7:14025907-14025957	Caco-2	colon:	n/a
26	chr7:14025907-14025957	NH-A	brain:	n/a
27	chr7:14025907-14025957	IMR90	lung:	fetal
28	chr7:14025907-14025957	PANC-1	pancreas:	n/a
29	chr7:14025907-14025957	HepG2	liver:	n/a
30	chr7:14025907-14025957	BJ	skin:	n/a
31	chr7:14025907-14025957	HCF	heart:	n/a
32	chr7:14025907-14025957	ECC-1	luminal epithelium:	n/a
33	chr7:14025907-14025957	RPTEC	kidney:	n/a
34	chr7:14025907-14025957	GM06990	blood:	n/a
35	chr7:14025907-14025957	HCT-116	colon:	n/a
36	chr7:14025907-14025957	GM12891	blood:	n/a
37	chr7:14025907-14025957	U87	brain:	n/a
38	chr7:14025907-14025957	BE2_C	brain:	n/a
39	chr7:14025907-14025957	K562	blood:	n/a
40	chr7:14025907-14025957	HUVEC	blood vessel:	n/a
41	chr7:14025907-14025957	MCF-7	breast:	n/a
42	chr7:14025907-14025957	SKMC	muscle:	n/a
43	chr7:14025907-14025957	HRPEpiC	eye:	n/a
44	chr7:14025907-14025957	LNCaP	prostate:	n/a
45	chr7:14025907-14025957	AoSMC	blood vessel:	n/a
46	chr7:14025907-14025957	HCPEpiC	choroid plexus:	n/a
47	chr7:14025907-14025957	HAEpiC	amniotic membrane:	n/a
48	chr7:14025907-14025957	H1-hESC	embryonic stem cell:	embryo
49	chr7:14025907-14025957	NHBE	bronchial:	n/a
50	chr7:14025907-14025957	HPAEpiC	pulmonary alveolar:	n/a

(count:44 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:13994487..13997447-chr7:13998861..14001557,3	K562	blood:
2	chr7:13985844..13987492-chr7:14019235..14021498,3	K562	blood:
3	chr7:14008374..14010454-chr7:14010741..14014267,3	K562	blood:
4	chr7:13997095..13998598-chr7:14011763..14014097,2	K562	blood:
5	chr7:13964325..13967217-chr7:14020611..14022495,2	K562	blood:
6	chr7:13980622..13983188-chr7:14022030..14023536,2	K562	blood:
7	chr7:14027263..14030675-chr7:14047798..14051480,3	K562	blood:
8	chr7:14000124..14001645-chr7:14029158..14031129,2	K562	blood:
9	chr7:14008374..14010454-chr7:14010741..14014267,3	K562	blood:
10	chr7:13998712..14001529-chr7:14011348..14014089,2	K562	blood:
11	chr7:13991446..13994404-chr7:14016165..14019066,2	K562	blood:
12	chr7:14007347..14010372-chr7:14013891..14016149,3	K562	blood:
13	chr7:13996982..14001014-chr7:14002058..14006442,5	K562	blood:
14	chr7:14006832..14009874-chr7:14010267..14013655,4	K562	blood:
15	chr7:14008558..14010409-chr7:14028328..14031106,2	K562	blood:
16	chr7:13996982..13998734-chr7:14003556..14005276,2	K562	blood:
17	chr7:13989697..13991875-chr7:13998508..14000403,2	K562	blood:
18	chr7:13997007..14000342-chr7:14017723..14020427,3	K562	blood:
19	chr7:13996982..13998734-chr7:14003556..14005276,2	K562	blood:
20	chr7:13972971..13975876-chr7:14017215..14019067,2	K562	blood:
21	chr7:14006507..14011484-chr7:14016197..14021172,5	K562	blood:
22	chr7:13987872..13991716-chr7:13991871..13996241,5	K562	blood:
23	chr7:13993113..13994903-chr7:14003071..14005104,2	K562	blood:
24	chr7:13998712..14001529-chr7:14011348..14014089,2	K562	blood:
25	chr7:14011992..14014933-chr7:14015921..14017592,2	K562	blood:
26	chr7:13989943..13991716-chr7:13993587..13996241,2	K562	blood:
27	chr7:14014823..14017219-chr7:14018906..14020830,2	MCF-7	breast:
28	chr7:13997566..14001513-chr7:14018273..14020813,4	K562	blood:
29	chr7:13997007..14000342-chr7:14017723..14020427,3	K562	blood:
30	chr7:13994487..13997447-chr7:13998861..14001557,3	K562	blood:
31	chr7:14006642..14008318-chr7:14033077..14034662,2	K562	blood:
32	chr7:13996982..14001014-chr7:14002058..14006442,5	K562	blood:
33	chr7:13997566..14001513-chr7:14018273..14020813,4	K562	blood:
34	chr7:14007601..14010058-chr7:14027934..14029828,2	K562	blood:
35	chr7:14007347..14010372-chr7:14013891..14016149,3	K562	blood:
36	chr7:14006832..14009874-chr7:14010267..14013655,4	K562	blood:
37	chr7:14016754..14019512-chr7:14048392..14050407,2	K562	blood:
38	chr7:13999444..14001578-chr7:14011983..14013986,2	K562	blood:
39	chr7:13997095..13998598-chr7:14011763..14014097,2	K562	blood:
40	chr7:14011992..14014933-chr7:14015921..14017592,2	K562	blood:
41	chr7:14014823..14017219-chr7:14018906..14020830,2	MCF-7	breast:
42	chr7:14006507..14011484-chr7:14016197..14021172,5	K562	blood:
43	chr7:13989697..13992273-chr7:13998903..14000492,2	K562	blood:
44	chr7:13999444..14001578-chr7:14011983..14013986,2	K562	blood:

No data

Variant related genes	Relation type
ETV1	TF binding region
ETV1	CpG island
ENSG00000252374	chromatin interactions
ENSG00000006468	chromatin interactions

Extended variants
information (count: 1417 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:1417 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7800918	chr7:13995209-13995210	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs578020136	chr7:13995218-13995219	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs543572352	chr7:13995227-13995228	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs146831684	chr7:13995247-13995248	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs573764630	chr7:13995323-13995324	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs139264167	chr7:13995421-13995422	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs535801946	chr7:13995461-13995462	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs559220315	chr7:13995467-13995468	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs572830396	chr7:13995468-13995469	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs59437625	chr7:13995484-13995485	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs541085092	chr7:13995504-13995505	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs7804410	chr7:13995524-13995525	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs564745728	chr7:13995564-13995565	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs76189242	chr7:13995569-13995570	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs368204624	chr7:13995573-13995574	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs550410535	chr7:13995604-13995605	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs561077773	chr7:13995661-13995662	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs73679051	chr7:13995673-13995674	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs549623550	chr7:13995688-13995689	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs373320771	chr7:13995699-13995700	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs566360608	chr7:13995715-13995716	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs60787150	chr7:13995729-13995730	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs369515848	chr7:13995735-13995736	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs571552614	chr7:13995787-13995788	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs537512712	chr7:13995802-13995803	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs188411011	chr7:13995810-13995811	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs541563921	chr7:13995817-13995818	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs757701	chr7:13995818-13995819	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs536017214	chr7:13995821-13995822	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs150906656	chr7:13995849-13995850	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs373389016	chr7:13995860-13995861	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs3801100	chr7:13995882-13995883	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs62454609	chr7:13995883-13995884	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs564854092	chr7:13995904-13995905	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs192643652	chr7:13995910-13995911	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs149257268	chr7:13995930-13995931	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs576976597	chr7:13995946-13995947	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs545897419	chr7:13995987-13995988	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs377593456	chr7:13995998-13995999	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs113219883	chr7:13996011-13996012	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs79731879	chr7:13996024-13996025	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs560008147	chr7:13996061-13996062	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs528748894	chr7:13996062-13996063	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs570549987	chr7:13996146-13996147	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs79782775	chr7:13996163-13996164	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs541799225	chr7:13996230-13996231	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs562619214	chr7:13996264-13996265	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs78626285	chr7:13996295-13996296	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs183043907	chr7:13996384-13996385	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs567406781	chr7:13996412-13996413	Weak transcription	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
Renal cell carcinoma	18194544	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
Myelofibrosis	22110671	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	22522925	CNVD
Prostate cancer	21298110	CNVD
Glioblastoma multiforme	22122801	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Prostate cancer	17079440	CNVD
Pancreatic cancer	17952125	CNVD
Glioblastoma multiforme	18628472	CNVD

Chromatin state (count:661 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:13975600-14003600	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr7:13975600-14003600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr7:13975600-14013800	Weak transcription	Left Ventricle	heart
4	chr7:13978800-14004600	Weak transcription	Fetal Lung	lung
5	chr7:13979200-13998000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr7:13985800-14004600	Weak transcription	NHLF	lung
7	chr7:13986200-13997000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr7:13988000-14012800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr7:13988200-14010400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr7:13989000-14019400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr7:13989400-14003600	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr7:13990000-13995600	Weak transcription	Pancreatic Islets	Pancreatic Islet
13	chr7:13990000-14003400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr7:13990000-14003600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr7:13990200-13996200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr7:13990200-13997200	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr7:13990400-13997800	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr7:13990800-14014000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr7:13990800-14014400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr7:13994200-13995600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr7:13994600-13996000	Weak transcription	Fetal Heart	heart
22	chr7:13994600-13997000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
23	chr7:13995200-13995600	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr7:13995200-13996000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr7:13995200-13997200	Weak transcription	Cortex derived primary cultured neurospheres	brain
26	chr7:13995600-13995800	Enhancers	Pancreatic Islets	Pancreatic Islet
27	chr7:13995600-13996000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr7:13995600-13997000	Weak transcription	HUES48 Cell Line	embryonic stem cell
29	chr7:13995800-13996000	Weak transcription	Pancreatic Islets	Pancreatic Islet
30	chr7:13996000-13996400	Enhancers	Fetal Heart	heart
31	chr7:13996000-13997000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr7:13996000-13997200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr7:13996200-13996400	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr7:13996400-14011000	Weak transcription	Fetal Heart	heart
35	chr7:13997000-13997800	Strong transcription	HUES48 Cell Line	embryonic stem cell
36	chr7:13997000-13998200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr7:13997000-13998600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
38	chr7:13997000-13999000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr7:13997200-13997600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr7:13997200-13998000	Strong transcription	HUES64 Cell Line	embryonic stem cell
41	chr7:13997200-14000000	Strong transcription	Cortex derived primary cultured neurospheres	brain
42	chr7:13997600-14003600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr7:13997800-13998400	Strong transcription	HUES6 Cell Line	embryonic stem cell
44	chr7:13997800-14003400	Weak transcription	HUES48 Cell Line	embryonic stem cell
45	chr7:13998000-13998600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
46	chr7:13998000-14003400	Weak transcription	HUES64 Cell Line	embryonic stem cell
47	chr7:13998200-14009800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr7:13998400-14003400	Weak transcription	HUES6 Cell Line	embryonic stem cell
49	chr7:13998600-14003400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
50	chr7:13998600-14014000	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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