Variant report

Variant	nsv887756
Chromosome Location	chr7:16520193-16566391
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:292)
CpG islands
(count:489)
Chromatin interactive
region (count:33)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:292 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:16532091-16532676	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:16524530-16524826	HepG2	liver:	n/a	n/a
3	ATF1	chr7:16532120-16532671	K562	blood:	n/a	n/a
4	ATF1	chr7:16524430-16524691	K562	blood:	n/a	n/a
5	BACH1	chr7:16554096-16554182	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr7:16535740-16535854	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr7:16532148-16532511	HepG2	liver:	n/a	n/a
8	BHLHE40	chr7:16560820-16560829	K562	blood:	n/a	n/a
9	BHLHE40	chr7:16549629-16549783	K562	blood:	n/a	n/a
10	CBX3	chr7:16546083-16546469	K562	blood:	n/a	n/a
11	CBX3	chr7:16524140-16524868	HCT-116	colon:	n/a	n/a
12	CBX3	chr7:16524126-16524955	HCT-116	colon:	n/a	n/a
13	CBX3	chr7:16541509-16541827	K562	blood:	n/a	n/a
14	CCNT2	chr7:16532206-16532616	K562	blood:	n/a	n/a
15	CCNT2	chr7:16551678-16551771	K562	blood:	n/a	n/a
16	CCNT2	chr7:16533597-16533769	K562	blood:	n/a	n/a
17	CEBPB	chr7:16547194-16547217	K562	blood:	n/a	n/a
18	CEBPB	chr7:16529722-16529727	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr7:16546212-16546248	K562	blood:	n/a	n/a
20	CEBPB	chr7:16563972-16564346	MCF-7	breast:	n/a	n/a
21	CEBPB	chr7:16532195-16532520	HepG2	liver:	n/a	n/a
22	CEBPB	chr7:16529660-16529787	K562	blood:	n/a	n/a
23	CEBPB	chr7:16532330-16532712	K562	blood:	n/a	n/a
24	CEBPB	chr7:16531125-16531360	K562	blood:	n/a	chr7:16531240-16531251
25	CEBPB	chr7:16524110-16525044	HCT-116	colon:	n/a	n/a
26	CHD2	chr7:16532233-16532572	HepG2	liver:	n/a	n/a
27	CTCF	chr7:16559379-16559405	GM10248	blood:	n/a	n/a
28	CTCF	chr7:16549600-16549750	HRPEpiC	eye:	n/a	chr7:16549697-16549715
29	CTCF	chr7:16529800-16529950	GM06990	blood:	n/a	n/a
30	CTCF	chr7:16549597-16549793	MCF-7	breast:	n/a	chr7:16549697-16549715
31	CTCF	chr7:16549510-16549922	MCF-7	breast:	n/a	chr7:16549697-16549715
32	CTCF	chr7:16549560-16549710	SK-N-SH_RA	brain:	n/a	n/a
33	CTCF	chr7:16549660-16549810	HPF	lung:	n/a	chr7:16549697-16549715
34	CTCF	chr7:16549516-16549838	K562	blood:	n/a	chr7:16549697-16549715
35	CTCF	chr7:16549601-16549785	K562	blood:	n/a	chr7:16549697-16549715
36	CTCF	chr7:16549880-16550030	HFF-Myc	foreskin:	n/a	n/a
37	CTCF	chr7:16549560-16549710	GM12872	blood:	n/a	n/a
38	CTCF	chr7:16549620-16549770	HCPEpiC	choroid plexus:	n/a	chr7:16549697-16549715
39	CTCF	chr7:16549580-16549730	HEK293	kidney:	n/a	chr7:16549697-16549715
40	CTCF	chr7:16559883-16559921	GM20000	blood:	n/a	n/a
41	CTCF	chr7:16549700-16549850	BE2_C	brain:	n/a	n/a
42	CTCF	chr7:16549520-16549670	MCF-7	breast:	n/a	n/a
43	CTCF	chr7:16549580-16549730	HPAF	blood vessel:	n/a	chr7:16549697-16549715
44	CTCF	chr7:16549400-16549871	K562	blood:	n/a	chr7:16549697-16549715 chr7:16549429-16549437
45	CTCF	chr7:16549480-16549630	HFF-Myc	foreskin:	n/a	n/a
46	CTCF	chr7:16549560-16549710	K562	blood:	n/a	n/a
47	CTCF	chr7:16549600-16549750	HA-sp	spinal cord:	n/a	chr7:16549697-16549715
48	CTCF	chr7:16549560-16549710	MCF-7	breast:	n/a	n/a
49	CTCF	chr7:16549660-16549810	HCT-116	colon:	n/a	chr7:16549697-16549715
50	CTCF	chr7:16549621-16549706	HepG2	liver:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:16551452-16551502	HRE	kidney:	n/a
2	chr7:16551452-16551502	HRE	kidney:	n/a
3	chr7:16542008-16542058	SK-N-MC	brain:	n/a
4	chr7:16524513-16524563	SK-N-MC	brain:	n/a
5	chr7:16524513-16524563	AoSMC	blood vessel:	n/a
6	chr7:16551452-16551502	Jurkat	blood:	n/a
7	chr7:16542008-16542058	HL-60	blood:	n/a
8	chr7:16565197-16565247	Hepatocyte	liver:	n/a
9	chr7:16542008-16542058	SK-N-SH_RA	brain:	n/a
10	chr7:16566261-16566311	SK-N-SH	brain:	n/a
11	chr7:16565197-16565247	GM06990	blood:	n/a
12	chr7:16524513-16524563	GM12878	blood:	n/a
13	chr7:16566261-16566311	Hela-S3	cervix:	n/a
14	chr7:16542008-16542058	MCF10A-Er-Src	breast:	n/a
15	chr7:16524513-16524563	PANC-1	pancreas:	n/a
16	chr7:16565197-16565247	BE2_C	brain:	n/a
17	chr7:16565197-16565247	AoSMC	blood vessel:	n/a
18	chr7:16565197-16565247	HPAEpiC	pulmonary alveolar:	n/a
19	chr7:16524513-16524563	HAEpiC	amniotic membrane:	n/a
20	chr7:16551452-16551502	AG09309	skin:	n/a
21	chr7:16566261-16566311	GM12892	blood:	n/a
22	chr7:16542142-16542192	SK-N-SH_RA	brain:	n/a
23	chr7:16566261-16566311	Caco-2	colon:	n/a
24	chr7:16566261-16566311	HMEC	breast:	n/a
25	chr7:16542008-16542058	IMR90	lung:	fetal
26	chr7:16551452-16551502	HCT-116	colon:	n/a
27	chr7:16541901-16541951	AoSMC	blood vessel:	n/a
28	chr7:16562910-16562960	H1-hESC	embryonic stem cell:	embryo
29	chr7:16562910-16562960	GM06990	blood:	n/a
30	chr7:16566261-16566311	AG04449	skin:	fetal
31	chr7:16524513-16524563	K562	blood:	n/a
32	chr7:16541901-16541951	HEK293	kidney:	embryo
33	chr7:16565197-16565247	HUVEC	blood vessel:	n/a
34	chr7:16565197-16565247	GM19239	blood:	n/a
35	chr7:16565197-16565247	HCT-116	colon:	n/a
36	chr7:16541901-16541951	HMEC	breast:	n/a
37	chr7:16542008-16542058	AG09309	skin:	n/a
38	chr7:16541901-16541951	CMK	blood:	n/a
39	chr7:16542142-16542192	GM12891	blood:	n/a
40	chr7:16565197-16565247	GM12878	blood:	n/a
41	chr7:16541901-16541951	U87	brain:	n/a
42	chr7:16541901-16541951	HCM	heart:	n/a
43	chr7:16542008-16542058	K562	blood:	n/a
44	chr7:16524513-16524563	MCF10A-Er-Src	breast:	n/a
45	chr7:16562910-16562960	Jurkat	blood:	n/a
46	chr7:16566261-16566311	NHDF-neo	bronchial:	n/a
47	chr7:16524513-16524563	AG09309	skin:	n/a
48	chr7:16541901-16541951	NH-A	brain:	n/a
49	chr7:16562910-16562960	HCF	heart:	n/a
50	chr7:16542008-16542058	HNPCEpiC	eye:	n/a

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:16521718..16524070-chr7:16531143..16534278,3	K562	blood:
2	chr7:16504445..16506740-chr7:16521593..16524423,2	K562	blood:
3	chr7:16530699..16533769-chr7:16536615..16539765,3	K562	blood:
4	chr7:16557755..16560171-chr7:16565512..16568469,2	K562	blood:
5	chr7:16521718..16524070-chr7:16531143..16534278,3	K562	blood:
6	chr7:16536910..16539248-chr7:16549389..16552367,2	K562	blood:
7	chr7:16556554..16559234-chr7:16561265..16563512,3	K562	blood:
8	chr7:16558907..16560805-chr7:16603285..16605880,2	K562	blood:
9	chr7:16518789..16520770-chr7:16521668..16524665,2	K562	blood:
10	chr7:16532269..16535153-chr7:16538265..16540761,2	K562	blood:
11	chr7:16531650..16533232-chr7:16685013..16686777,2	K562	blood:
12	chr7:16530699..16533769-chr7:16536615..16539765,3	K562	blood:
13	chr7:16499530..16502497-chr7:16557938..16560776,2	K562	blood:
14	chr7:16532273..16538122-chr7:16541684..16545324,6	K562	blood:
15	chr7:16556554..16559234-chr7:16561265..16563512,3	K562	blood:
16	chr7:16523356..16525070-chr7:16684503..16686838,2	MCF-7	breast:
17	chr7:16532204..16534776-chr7:16581975..16583734,2	K562	blood:
18	chr7:16515092..16517007-chr7:16528168..16530521,2	K562	blood:
19	chr7:16556554..16559185-chr7:16561265..16563512,2	K562	blood:
20	chr7:16532273..16538122-chr7:16541684..16545324,6	K562	blood:
21	chr7:16503947..16506653-chr7:16549566..16552507,2	K562	blood:
22	chr7:16491075..16493101-chr7:16549176..16551886,2	K562	blood:
23	chr7:16556554..16559185-chr7:16561265..16563512,2	K562	blood:
24	chr7:16536910..16539248-chr7:16549389..16552367,2	K562	blood:
25	chr7:16507602..16510153-chr7:16537013..16538604,2	K562	blood:
26	chr7:16460296..16463225-chr7:16547854..16549710,2	K562	blood:
27	chr7:16518789..16520770-chr7:16521668..16524665,2	K562	blood:
28	chr7:16526991..16528708-chr7:16530657..16533220,2	K562	blood:
29	chr7:16135393..16137832-chr7:16533811..16535542,2	K562	blood:
30	chr7:16503625..16506549-chr7:16546655..16549241,2	K562	blood:
31	chr7:16526991..16528708-chr7:16530657..16533220,2	K562	blood:
32	chr7:16532269..16535153-chr7:16538265..16540761,2	K562	blood:
33	chr7:16541764..16543628-chr7:16604079..16606221,2	K562	blood:

No data

Variant related genes	Relation type
LRRC72	TF binding region
LRRC72	CpG island
ENSG00000205858	chromatin interactions
ENSG00000136261	chromatin interactions
ENSG00000214960	chromatin interactions
ENSG00000171243	chromatin interactions
ENSG00000106524	chromatin interactions

Extended variants
information (count: 1997 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:1997 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2704668	chr7:16520193-16520194	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs575643476	chr7:16520263-16520264	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs56227196	chr7:16520361-16520362	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs182910692	chr7:16520397-16520398	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs545169495	chr7:16520441-16520442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs2528466	chr7:16520450-16520451	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs186504908	chr7:16520463-16520464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs548681473	chr7:16520468-16520469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs546942966	chr7:16520505-16520506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs566880137	chr7:16520525-16520526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs115253371	chr7:16520550-16520551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs191697464	chr7:16520575-16520576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs148627384	chr7:16520587-16520588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs374230437	chr7:16520623-16520624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs530477411	chr7:16520627-16520628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs552161874	chr7:16520668-16520669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs77439877	chr7:16520673-16520674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs182707392	chr7:16520696-16520697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs371167825	chr7:16520734-16520735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs114404384	chr7:16520743-16520744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs568001137	chr7:16520782-16520783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs535308982	chr7:16520789-16520790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs556688498	chr7:16520843-16520844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs569341352	chr7:16520860-16520861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs114970014	chr7:16520869-16520870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs2528465	chr7:16520887-16520888	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs186978351	chr7:16520900-16520901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs552650305	chr7:16520902-16520903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs559392435	chr7:16520903-16520904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs193191833	chr7:16520943-16520944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs556136882	chr7:16520987-16520988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs185093797	chr7:16521000-16521001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs544823933	chr7:16521035-16521036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs75017442	chr7:16521042-16521043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs142168381	chr7:16521043-16521044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs548098582	chr7:16521051-16521052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs146725603	chr7:16521067-16521068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs73306293	chr7:16521091-16521092	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs144142065	chr7:16521103-16521104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs546182613	chr7:16521118-16521119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs561648344	chr7:16521127-16521128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs529110125	chr7:16521131-16521132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs2704669	chr7:16521181-16521182	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs199899930	chr7:16521190-16521191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs568928673	chr7:16521200-16521201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs200327359	chr7:16521231-16521232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs189134329	chr7:16521275-16521276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs570897707	chr7:16521335-16521336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs551617180	chr7:16521341-16521342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs193027018	chr7:16521357-16521358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

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
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
Bladder cancer	21909424	CNVD
Cancer	21183584	CNVD
Autism	20808228	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:185 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:16512400-16524200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr7:16519000-16520400	Enhancers	Fetal Lung	lung
3	chr7:16519200-16524200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr7:16519800-16526800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr7:16523600-16525600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr7:16523600-16525800	Enhancers	HMEC	breast
7	chr7:16523800-16524200	Enhancers	A549	lung
8	chr7:16523800-16524800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr7:16523800-16525600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr7:16524000-16524200	Enhancers	NH-A	brain
11	chr7:16524000-16525000	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr7:16524000-16525400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr7:16524000-16525400	Enhancers	NHEK	skin
14	chr7:16524000-16525600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr7:16524000-16525800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr7:16524200-16524400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr7:16524200-16524400	Enhancers	Fetal Intestine Small	intestine
18	chr7:16524200-16524400	Enhancers	Pancreas	Pancrea
19	chr7:16524200-16524600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr7:16524200-16524600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr7:16524200-16524600	Enhancers	Fetal Intestine Large	intestine
22	chr7:16524200-16524600	Flanking Active TSS	NH-A	brain
23	chr7:16524200-16524800	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr7:16524200-16524800	Enhancers	H1 Cell Line	embryonic stem cell
25	chr7:16524200-16524800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr7:16524200-16524800	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr7:16524200-16524800	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr7:16524200-16524800	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr7:16524200-16524800	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr7:16524200-16524800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr7:16524200-16524800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr7:16524200-16525000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr7:16524200-16525000	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr7:16524200-16525000	Flanking Active TSS	A549	lung
35	chr7:16524200-16525200	Enhancers	Breast Myoepithelial Primary Cells	Breast
36	chr7:16524200-16525200	Enhancers	HepG2	liver
37	chr7:16524200-16525200	Enhancers	K562	blood
38	chr7:16524200-16525400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr7:16524400-16524800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr7:16524600-16524800	Weak transcription	Fetal Intestine Large	intestine
41	chr7:16524600-16525000	Enhancers	Muscle Satellite Cultured Cells	--
42	chr7:16524600-16525200	Enhancers	NH-A	brain
43	chr7:16524600-16528000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr7:16524800-16525200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr7:16524800-16525200	Enhancers	Fetal Intestine Large	intestine
46	chr7:16524800-16526600	Weak transcription	Pancreas	Pancrea
47	chr7:16524800-16533400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr7:16525000-16525600	Enhancers	A549	lung
49	chr7:16525000-16528000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr7:16525200-16529600	Weak transcription	HepG2	liver

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