Variant report

Variant	nsv887967
Chromosome Location	chr7:39009307-39090698
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:249)
CpG islands
(count:1037)
Chromatin interactive
region (count:29)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:249 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:39056169-39056356	HepG2	liver:	n/a	n/a
2	ATF1	chr7:39013500-39013605	K562	blood:	n/a	n/a
3	BACH1	chr7:39013444-39013640	H1-hESC	embryonic stem cell:	n/a	chr7:39013572-39013586
4	BHLHE40	chr7:39056365-39056469	K562	blood:	n/a	n/a
5	BRCA1	chr7:39015706-39015860	H1-hESC	embryonic stem cell:	n/a	n/a
6	CCNT2	chr7:39077221-39077330	K562	blood:	n/a	n/a
7	CCNT2	chr7:39015611-39015783	K562	blood:	n/a	n/a
8	CEBPB	chr7:39062999-39063139	HepG2	liver:	n/a	n/a
9	CEBPB	chr7:39035239-39035457	A549	lung:	n/a	n/a
10	CEBPB	chr7:39032904-39033093	K562	blood:	n/a	n/a
11	CEBPB	chr7:39076453-39076716	HepG2	liver:	n/a	chr7:39076586-39076597 chr7:39076627-39076640
12	CEBPB	chr7:39062909-39063204	MCF-7	breast:	n/a	n/a
13	CEBPB	chr7:39016200-39016457	IMR90	lung:	n/a	chr7:39016341-39016354 chr7:39016341-39016352 chr7:39016342-39016353 chr7:39016341-39016354 chr7:39016341-39016354
14	CEBPB	chr7:39032925-39033063	HepG2	liver:	n/a	n/a
15	CEBPB	chr7:39062990-39063177	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr7:39039920-39040082	IMR90	lung:	n/a	n/a
17	CEBPB	chr7:39032894-39033177	IMR90	lung:	n/a	n/a
18	CEBPB	chr7:39062950-39063157	K562	blood:	n/a	n/a
19	CEBPB	chr7:39016175-39016456	H1-hESC	embryonic stem cell:	n/a	chr7:39016341-39016354 chr7:39016341-39016352 chr7:39016342-39016353 chr7:39016341-39016354 chr7:39016341-39016354
20	CEBPB	chr7:39076515-39076729	A549	lung:	n/a	chr7:39076586-39076597 chr7:39076627-39076640
21	CEBPB	chr7:39016240-39016481	HepG2	liver:	n/a	chr7:39016341-39016354 chr7:39016341-39016352 chr7:39016342-39016353 chr7:39016341-39016354 chr7:39016341-39016354
22	CEBPB	chr7:39016181-39016514	K562	blood:	n/a	chr7:39016341-39016354 chr7:39016341-39016352 chr7:39016342-39016353 chr7:39016341-39016354 chr7:39016341-39016354
23	CHD1	chr7:39015665-39015838	H1-hESC	embryonic stem cell:	n/a	chr7:39015794-39015804
24	CHD2	chr7:39015585-39015825	H1-hESC	embryonic stem cell:	n/a	chr7:39015794-39015804
25	CTCF	chr7:39010060-39010210	MCF-7	breast:	n/a	n/a
26	CTCF	chr7:39030600-39030750	HCPEpiC	choroid plexus:	n/a	chr7:39030671-39030681
27	CTCF	chr7:39010100-39010250	K562	blood:	n/a	n/a
28	CTCF	chr7:39041417-39041504	GM19239	blood:	n/a	n/a
29	CTCF	chr7:39010055-39010180	K562	blood:	n/a	n/a
30	CTCF	chr7:39010040-39010190	NHEK	skin:	n/a	n/a
31	CTCF	chr7:39030428-39030898	HCT-116	colon:	n/a	chr7:39030671-39030681
32	CTCF	chr7:39010020-39010170	SK-N-SH_RA	brain:	n/a	n/a
33	CTCF	chr7:39009992-39010279	K562	blood:	n/a	n/a
34	CTCF	chr7:39009980-39010130	HBMEC	blood vessel:	n/a	n/a
35	CTCF	chr7:39088360-39088375	GM10266	blood:	n/a	n/a
36	CTCF	chr7:39010100-39010250	HCT-116	colon:	n/a	n/a
37	CTCF	chr7:39030600-39030750	AG04450	lung:	n/a	chr7:39030671-39030681
38	CTCF	chr7:39015648-39015762	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr7:39041398-39041416	GM19239	blood:	n/a	n/a
40	CTCF	chr7:39015787-39015993	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr7:39010060-39010210	NB4	blood:	n/a	n/a
42	CTCF	chr7:39010020-39010170	HEK293	kidney:	n/a	n/a
43	CTCF	chr7:39010060-39010210	GM12872	blood:	n/a	n/a
44	CTCF	chr7:39010120-39010270	GM12873	blood:	n/a	n/a
45	CTCF	chr7:39041376-39041464	MCF-7	breast:	n/a	n/a
46	CTCF	chr7:39010040-39010190	K562	blood:	n/a	n/a
47	CTCF	chr7:39010060-39010210	BE2_C	brain:	n/a	n/a
48	CTCF	chr7:39010040-39010190	Caco-2	colon:	n/a	n/a
49	CTCF	chr7:39009980-39010130	HCFaa	heart:	n/a	n/a
50	CTCF	chr7:39010000-39010150	GM12865	blood:	n/a	n/a

(count:1037 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:39074034-39074084	HEEpiC	esophagus:	n/a
2	chr7:39045789-39045839	PrEC	prostate:	n/a
3	chr7:39017305-39017355	PANC-1	pancreas:	n/a
4	chr7:39015928-39015978	SAEC	small airway:	n/a
5	chr7:39017305-39017355	HIPEpiC	eye:	n/a
6	chr7:39015705-39015755	HEK293	kidney:	embryo
7	chr7:39015705-39015755	MCF10A-Er-Src	breast:	n/a
8	chr7:39074034-39074084	HNPCEpiC	eye:	n/a
9	chr7:39053253-39053303	T-47D	breast:	n/a
10	chr7:39053253-39053303	MCF10A-Er-Src	breast:	n/a
11	chr7:39056400-39056450	GM12891	blood:	n/a
12	chr7:39017305-39017355	HepG2	liver:	n/a
13	chr7:39082429-39082479	NT2-D1	testis:	n/a
14	chr7:39015544-39015594	K562	blood:	n/a
15	chr7:39015705-39015755	Jurkat	blood:	n/a
16	chr7:39082429-39082479	ProgFib	skin:	n/a
17	chr7:39017305-39017355	HCF	heart:	n/a
18	chr7:39051529-39051579	H1-hESC	embryonic stem cell:	embryo
19	chr7:39044924-39044974	Hepatocyte	liver:	n/a
20	chr7:39056400-39056450	HL-60	blood:	n/a
21	chr7:39013676-39013726	NHBE	bronchial:	n/a
22	chr7:39045789-39045839	PANC-1	pancreas:	n/a
23	chr7:39017305-39017355	NH-A	brain:	n/a
24	chr7:39015544-39015594	AG04449	skin:	fetal
25	chr7:39015544-39015594	HEK293	kidney:	embryo
26	chr7:39051529-39051579	GM12892	blood:	n/a
27	chr7:39015705-39015755	U87	brain:	n/a
28	chr7:39017630-39017680	HUVEC	blood vessel:	n/a
29	chr7:39056400-39056450	NB4	blood:	n/a
30	chr7:39017455-39017505	IMR90	lung:	fetal
31	chr7:39017305-39017355	AG09319	gingival:	n/a
32	chr7:39013676-39013726	T-47D	breast:	n/a
33	chr7:39082429-39082479	AG09309	skin:	n/a
34	chr7:39015544-39015594	GM12891	blood:	n/a
35	chr7:39053253-39053303	HCF	heart:	n/a
36	chr7:39082429-39082479	Caco-2	colon:	n/a
37	chr7:39015705-39015755	AG10803	skin:	n/a
38	chr7:39017630-39017680	AoSMC	blood vessel:	n/a
39	chr7:39017630-39017680	SK-N-SH	brain:	n/a
40	chr7:39053253-39053303	HEEpiC	esophagus:	n/a
41	chr7:39051529-39051579	MCF10A-Er-Src	breast:	n/a
42	chr7:39018178-39018228	Hela-S3	cervix:	n/a
43	chr7:39015544-39015594	HMEC	breast:	n/a
44	chr7:39046213-39046263	Hepatocyte	liver:	n/a
45	chr7:39082429-39082479	SK-N-SH_RA	brain:	n/a
46	chr7:39015544-39015594	HCT-116	colon:	n/a
47	chr7:39074034-39074084	NH-A	brain:	n/a
48	chr7:39044924-39044974	IMR90	lung:	fetal
49	chr7:39016050-39016100	PFSK-1	brain:	n/a
50	chr7:39017455-39017505	HCF	heart:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:39053567..39055132-chr7:39055413..39056943,2	K562	blood:
2	chr7:39067188..39069142-chr7:39090366..39092625,2	K562	blood:
3	chr7:39005474..39007297-chr7:39033578..39035235,2	K562	blood:
4	chr7:38835380..38837866-chr7:39068899..39071738,2	K562	blood:
5	chr7:39018323..39020191-chr7:39020334..39022655,2	MCF-7	breast:
6	chr7:39056885..39058530-chr7:39059051..39061943,3	K562	blood:
7	chr7:39035446..39037795-chr7:39039959..39041669,2	K562	blood:
8	chr7:39067188..39069142-chr7:39090366..39092625,2	K562	blood:
9	chr7:39056516..39058385-chr7:39059051..39061295,2	K562	blood:
10	chr7:39068242..39069877-chr7:39078020..39079594,2	K562	blood:
11	chr7:39007202..39009703-chr7:39021653..39023685,2	K562	blood:
12	chr7:39059555..39062037-chr7:39102548..39105141,2	K562	blood:
13	chr7:39035446..39037795-chr7:39039959..39041669,2	K562	blood:
14	chr7:39052158..39055296-chr7:39055387..39058245,4	K562	blood:
15	chr7:39044098..39047140-chr7:39057342..39060274,3	K562	blood:
16	chr7:39056885..39058530-chr7:39059051..39061943,3	K562	blood:
17	chr7:39053567..39055132-chr7:39055413..39056943,2	K562	blood:
18	chr7:39077523..39079724-chr7:39083023..39084974,2	K562	blood:
19	chr7:39010566..39013260-chr7:39044087..39046092,2	K562	blood:
20	chr7:39018323..39020191-chr7:39020334..39022655,2	MCF-7	breast:
21	chr7:39007202..39009703-chr7:39021653..39023685,2	K562	blood:
22	chr7:39084602..39087149-chr7:39099410..39101801,2	K562	blood:
23	chr7:39030343..39033079-chr7:39034482..39036746,2	K562	blood:
24	chr7:39010566..39013260-chr7:39044087..39046092,2	K562	blood:
25	chr7:39056516..39058385-chr7:39059051..39061295,2	K562	blood:
26	chr7:39030343..39033079-chr7:39034482..39036746,2	K562	blood:
27	chr7:39014833..39018205-chr7:39019713..39022861,3	K562	blood:
28	chr7:39077523..39079724-chr7:39083023..39084974,2	K562	blood:
29	chr7:39068242..39069877-chr7:39078020..39079594,2	K562	blood:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-VPS41-1	chr7:39019495-39021106	NONHSAT120194
2	lnc-VPS41-1	chr7:39028235-39028353	NONHSAT120194
3	lnc-VPS41-1	chr7:39023843-39024005	ENSG00000233854
4	lnc-VPS41-1	chr7:39053013-39053168	NONHSAT120194
5	lnc-VPS41-1	chr7:39053057-39053151	ENSG00000233854
6	lnc-VPS41-1	chr7:39024477-39024521	NONHSAT120194
7	lnc-VPS41-1	chr7:39041720-39041818	NONHSAT120194
8	lnc-VPS41-1	chr7:39044663-39044812	ENSG00000233854
9	lnc-VPS41-1	chr7:39023850-39024005	NONHSAT120194
10	lnc-VPS41-1	chr7:39041612-39041672	ENSG00000233854
11	lnc-VPS41-1	chr7:39024477-39024521	ENSG00000233854
12	lnc-VPS41-1	chr7:39044663-39044812	NONHSAT120194
13	lnc-YAE1D1-4	chr7:39041329-39041554	NONHSAT120196

No data

Variant related genes	Relation type
POU6F2	TF binding region
POU6F2-AS2	TF binding region
POU6F2	CpG island
POU6F2-AS2	CpG island
ENSG00000006715	chromatin interactions
ENSG00000106536	chromatin interactions
ENSG00000233854	chromatin interactions

Extended variants
information (count: 2291 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:2291 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs116829583	chr7:39013206-39013207	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs183250876	chr7:39013230-39013231	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs555455889	chr7:39013235-39013236	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs117670105	chr7:39013236-39013237	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs534799744	chr7:39013244-39013245	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs113672745	chr7:39013260-39013261	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs367716829	chr7:39013286-39013287	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs187422845	chr7:39013298-39013299	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs563540261	chr7:39013324-39013325	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs113325812	chr7:39013332-39013333	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs369391266	chr7:39013365-39013366	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs542934451	chr7:39013420-39013421	Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs573683407	chr7:39013463-39013464	Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs559081240	chr7:39013475-39013476	Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs191558404	chr7:39013518-39013519	Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs529666380	chr7:39013521-39013522	Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs138635193	chr7:39013580-39013581	Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs554251732	chr7:39013588-39013589	Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs149314586	chr7:39013595-39013596	Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs35007470	chr7:39013634-39013635	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs549948105	chr7:39013635-39013636	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs112977398	chr7:39013676-39013677	Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
23	rs535772159	chr7:39013719-39013720	Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
24	rs549691355	chr7:39013723-39013724	Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
25	rs71548644	chr7:39013734-39013735	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs75675142	chr7:39013755-39013756	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs548619973	chr7:39013756-39013757	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs398085735	chr7:39013765-39013766	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs62443600	chr7:39014606-39014607	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs574936322	chr7:39014621-39014622	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs549741933	chr7:39014662-39014663	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs376564208	chr7:39014688-39014689	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs118064324	chr7:39014790-39014791	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs529437388	chr7:39014798-39014799	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs543221573	chr7:39014802-39014803	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs149068736	chr7:39014820-39014821	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs143087179	chr7:39014849-39014850	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs552148096	chr7:39014854-39014855	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs538593395	chr7:39014912-39014913	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs193269124	chr7:39014940-39014941	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs530934243	chr7:39014963-39014964	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs550748659	chr7:39014972-39014973	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs567765635	chr7:39014985-39014986	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs536383491	chr7:39014996-39014997	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs553112532	chr7:39015003-39015004	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs112725181	chr7:39015033-39015034	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs538536936	chr7:39015038-39015039	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs141152458	chr7:39015071-39015072	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs552677152	chr7:39015171-39015172	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs112452719	chr7:39015172-39015173	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
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
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
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	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
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Prostate cancer	18632612	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Acute myeloid leukemia	17237825	CNVD
Breast cancer	17899364	CNVD
Breast cancer	20409316	CNVD
Acute monocytic leukemia	16498392	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Colorectal cancer	19455253	CNVD
Glioblastoma multiforme	22286061	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Sezary syndrome	18413736	CNVD
Gastric cancer	24379144	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:372 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:39013200-39013800	Enhancers	ES-I3 Cell Line	embryonic stem cell
2	chr7:39013400-39013600	Bivalent Enhancer	HSMMtube	muscle
3	chr7:39013600-39013800	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr7:39014600-39015000	Enhancers	Fetal Brain Female	brain
5	chr7:39014600-39015800	Enhancers	Fetal Brain Male	brain
6	chr7:39014800-39015000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr7:39015200-39015400	Enhancers	H9 Cell Line	embryonic stem cell
8	chr7:39015200-39015800	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
9	chr7:39015200-39015800	Active TSS	Stomach Smooth Muscle	stomach
10	chr7:39015200-39016000	Bivalent/Poised TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr7:39015200-39016200	Active TSS	Fetal Brain Female	brain
12	chr7:39015200-39016400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
13	chr7:39015200-39021200	Active TSS	Pancreatic Islets	Pancreatic Islet
14	chr7:39015400-39015600	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr7:39015400-39015600	Bivalent/Poised TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr7:39015400-39015600	Flanking Bivalent TSS/Enh	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr7:39015400-39015600	Bivalent/Poised TSS	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr7:39015400-39015600	Bivalent/Poised TSS	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr7:39015400-39015600	Active TSS	Liver	Liver
20	chr7:39015400-39015600	Active TSS	Brain Germinal Matrix	brain
21	chr7:39015400-39015600	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum
22	chr7:39015400-39015600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
23	chr7:39015400-39015600	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
24	chr7:39015400-39015800	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr7:39015400-39015800	Bivalent/Poised TSS	Fetal Muscle Leg	muscle
26	chr7:39015400-39015800	Active TSS	Pancreas	Pancrea
27	chr7:39015400-39015800	Active TSS	Rectal Smooth Muscle	rectum
28	chr7:39015400-39015800	Bivalent Enhancer	Right Ventricle	heart
29	chr7:39015400-39016000	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
30	chr7:39015400-39016000	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
31	chr7:39015400-39016000	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr7:39015400-39016000	Bivalent/Poised TSS	Right Atrium	heart
33	chr7:39015400-39016200	Active TSS	H9 Cell Line	embryonic stem cell
34	chr7:39015400-39016200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr7:39015400-39016200	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr7:39015400-39016200	Flanking Bivalent TSS/Enh	Cortex derived primary cultured neurospheres	brain
37	chr7:39015400-39016200	Active TSS	Aorta	Aorta
38	chr7:39015400-39016200	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
39	chr7:39015400-39016400	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
40	chr7:39015400-39016400	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
41	chr7:39015400-39016400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
42	chr7:39015600-39015800	Bivalent/Poised TSS	Muscle Satellite Cultured Cells	--
43	chr7:39015600-39015800	Bivalent/Poised TSS	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr7:39015600-39015800	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr7:39015600-39015800	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr7:39015600-39015800	Active TSS	Brain Angular Gyrus	brain
47	chr7:39015600-39015800	Active TSS	Brain Inferior Temporal Lobe	brain
48	chr7:39015600-39015800	Bivalent Enhancer	Esophagus	oesophagus
49	chr7:39015600-39015800	Bivalent/Poised TSS	Fetal Stomach	stomach
50	chr7:39015600-39015800	Flanking Bivalent TSS/Enh	Placenta Amnion	Placenta Amnion

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