Variant report

Variant	nsv831110
Chromosome Location	chr7:118543340-118739362
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:118605996-118606086	K562	blood:	n/a	n/a
2	ATF1	chr7:118609507-118609553	K562	blood:	n/a	n/a
3	ATF1	chr7:118549154-118549158	K562	blood:	n/a	n/a
4	BCL3	chr7:118650678-118650912	GM12878	blood:	n/a	n/a
5	BHLHE40	chr7:118640025-118640296	GM12878	blood:	n/a	n/a
6	CEBPB	chr7:118706103-118706303	A549	lung:	n/a	n/a
7	CEBPB	chr7:118713529-118713772	A549	lung:	n/a	chr7:118713628-118713641 chr7:118713591-118713604 chr7:118713668-118713679 chr7:118713628-118713639 chr7:118713630-118713641 chr7:118713591-118713603 chr7:118713668-118713681 chr7:118713628-118713641
8	CEBPB	chr7:118572185-118572434	H1-hESC	embryonic stem cell:	n/a	chr7:118572300-118572311 chr7:118572298-118572309
9	CEBPB	chr7:118552168-118552368	HepG2	liver:	n/a	chr7:118552250-118552261
10	CEBPB	chr7:118713490-118713806	HepG2	liver:	n/a	chr7:118713628-118713641 chr7:118713591-118713604 chr7:118713668-118713679 chr7:118713628-118713639 chr7:118713630-118713641 chr7:118713591-118713603 chr7:118713668-118713681 chr7:118713628-118713641
11	CEBPB	chr7:118635637-118635889	A549	lung:	n/a	n/a
12	CEBPB	chr7:118548314-118548527	MCF-7	breast:	n/a	chr7:118548398-118548409
13	CEBPB	chr7:118597665-118597936	HepG2	liver:	n/a	chr7:118597811-118597822
14	CEBPB	chr7:118631545-118631767	HepG2	liver:	n/a	chr7:118631682-118631693
15	CEBPB	chr7:118548258-118548571	IMR90	lung:	n/a	chr7:118548398-118548409
16	CEBPB	chr7:118548218-118548566	HepG2	liver:	n/a	chr7:118548398-118548409
17	CEBPB	chr7:118664287-118664601	A549	lung:	n/a	n/a
18	CEBPB	chr7:118548217-118548578	K562	blood:	n/a	chr7:118548398-118548409
19	CEBPB	chr7:118646259-118646292	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr7:118640929-118641155	A549	lung:	n/a	chr7:118641131-118641144
21	CEBPB	chr7:118548218-118548557	A549	lung:	n/a	chr7:118548398-118548409
22	CEBPB	chr7:118568797-118568997	K562	blood:	n/a	chr7:118568889-118568900 chr7:118568889-118568902 chr7:118568891-118568900
23	CEBPB	chr7:118548225-118548596	H1-hESC	embryonic stem cell:	n/a	chr7:118548398-118548409
24	CEBPB	chr7:118558763-118558904	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr7:118635617-118635965	HepG2	liver:	n/a	n/a
26	CEBPB	chr7:118635615-118635937	IMR90	lung:	n/a	n/a
27	CEBPB	chr7:118572120-118572404	HepG2	liver:	n/a	chr7:118572300-118572311 chr7:118572298-118572309
28	CEBPB	chr7:118686542-118686614	A549	lung:	n/a	n/a
29	CEBPB	chr7:118730966-118731278	Hela-S3	cervix:	n/a	chr7:118731238-118731251
30	CEBPB	chr7:118572135-118572418	A549	lung:	n/a	chr7:118572300-118572311 chr7:118572298-118572309
31	CEBPB	chr7:118568724-118569020	HepG2	liver:	n/a	chr7:118568889-118568900 chr7:118568889-118568902 chr7:118568891-118568900
32	CEBPB	chr7:118568719-118569041	IMR90	lung:	n/a	chr7:118568889-118568900 chr7:118568889-118568902 chr7:118568891-118568900
33	CEBPB	chr7:118576878-118576970	HepG2	liver:	n/a	chr7:118576956-118576967
34	CEBPB	chr7:118640833-118641182	HepG2	liver:	n/a	chr7:118641131-118641144
35	CTCF	chr7:118558760-118558910	RPTEC	kidney:	n/a	chr7:118558802-118558818 chr7:118558801-118558819 chr7:118558804-118558817 chr7:118558803-118558824
36	CTCF	chr7:118558713-118558878	Pancreas_OC	pancreas:	n/a	chr7:118558802-118558818 chr7:118558801-118558819 chr7:118558804-118558817 chr7:118558803-118558824
37	CTCF	chr7:118558737-118558908	ECC-1	luminal epithelium:	n/a	chr7:118558802-118558818 chr7:118558801-118558819 chr7:118558804-118558817 chr7:118558803-118558824
38	CTCF	chr7:118596548-118596575	HepG2	liver:	n/a	n/a
39	CTCF	chr7:118558675-118558937	Medullo	brain:	n/a	chr7:118558802-118558818 chr7:118558801-118558819 chr7:118558804-118558817 chr7:118558803-118558824
40	CTCF	chr7:118558720-118558870	HMF	breast:	n/a	chr7:118558802-118558818 chr7:118558801-118558819 chr7:118558804-118558817 chr7:118558803-118558824
41	CTCF	chr7:118558630-118558972	IMR90	lung:	n/a	chr7:118558802-118558818 chr7:118558801-118558819 chr7:118558804-118558817 chr7:118558803-118558824
42	CTCF	chr7:118558637-118558987	MCF-7	breast:	n/a	chr7:118558802-118558818 chr7:118558801-118558819 chr7:118558804-118558817 chr7:118558803-118558824
43	CTCF	chr7:118558660-118558810	HRPEpiC	eye:	n/a	n/a
44	CTCF	chr7:118614940-118615090	NHDF-neo	bronchial:	n/a	n/a
45	CTCF	chr7:118558700-118558850	HMEC	breast:	n/a	chr7:118558802-118558818 chr7:118558801-118558819 chr7:118558804-118558817 chr7:118558803-118558824
46	CTCF	chr7:118558680-118558830	HMF	breast:	n/a	chr7:118558802-118558818 chr7:118558801-118558819 chr7:118558804-118558817 chr7:118558803-118558824
47	CTCF	chr7:118558760-118558910	BE2_C	brain:	n/a	chr7:118558802-118558818 chr7:118558801-118558819 chr7:118558804-118558817 chr7:118558803-118558824
48	CTCF	chr7:118558720-118558870	NHEK	skin:	n/a	chr7:118558802-118558818 chr7:118558801-118558819 chr7:118558804-118558817 chr7:118558803-118558824
49	CTCF	chr7:118558740-118558890	RPTEC	kidney:	n/a	chr7:118558802-118558818 chr7:118558801-118558819 chr7:118558804-118558817 chr7:118558803-118558824
50	CTCF	chr7:118736670-118736757	GM20000	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:118572128-118572178	HCM	heart:	n/a
2	chr7:118572128-118572178	HRPEpiC	eye:	n/a
3	chr7:118572128-118572178	HL-60	blood:	n/a
4	chr7:118572128-118572178	Jurkat	blood:	n/a
5	chr7:118572128-118572178	MCF-7	breast:	n/a
6	chr7:118572128-118572178	HMEC	breast:	n/a
7	chr7:118572128-118572178	AG04450	lung:	fetal
8	chr7:118572128-118572178	NHBE	bronchial:	n/a
9	chr7:118572128-118572178	HRE	kidney:	n/a
10	chr7:118572128-118572178	MCF10A-Er-Src	breast:	n/a
11	chr7:118572128-118572178	HRCEpiC	kidney:	n/a
12	chr7:118572128-118572178	A549	lung:	n/a
13	chr7:118572128-118572178	PFSK-1	brain:	n/a
14	chr7:118572128-118572178	PrEC	prostate:	n/a
15	chr7:118572128-118572178	AG04449	skin:	fetal
16	chr7:118572128-118572178	HPAEpiC	pulmonary alveolar:	n/a
17	chr7:118572128-118572178	Hepatocyte	liver:	n/a
18	chr7:118572128-118572178	NHDF-neo	bronchial:	n/a
19	chr7:118572128-118572178	AG10803	skin:	n/a
20	chr7:118572128-118572178	HCPEpiC	choroid plexus:	n/a
21	chr7:118572128-118572178	BE2_C	brain:	n/a
22	chr7:118572128-118572178	SK-N-MC	brain:	n/a
23	chr7:118572128-118572178	SK-N-SH	brain:	n/a
24	chr7:118572128-118572178	SK-N-SH_RA	brain:	n/a
25	chr7:118572128-118572178	RPTEC	kidney:	n/a
26	chr7:118572128-118572178	HIPEpiC	eye:	n/a
27	chr7:118572128-118572178	HNPCEpiC	eye:	n/a
28	chr7:118572128-118572178	HepG2	liver:	n/a
29	chr7:118572128-118572178	HAEpiC	amniotic membrane:	n/a
30	chr7:118572128-118572178	LNCaP	prostate:	n/a
31	chr7:118572128-118572178	NT2-D1	testis:	n/a
32	chr7:118572128-118572178	ECC-1	luminal epithelium:	n/a
33	chr7:118572128-118572178	AoSMC	blood vessel:	n/a
34	chr7:118572128-118572178	GM12892	blood:	n/a
35	chr7:118572128-118572178	HCF	heart:	n/a
36	chr7:118572128-118572178	Hela-S3	cervix:	n/a
37	chr7:118572128-118572178	GM12878	blood:	n/a
38	chr7:118572128-118572178	ovcar-3	ovarian:	n/a
39	chr7:118572128-118572178	Caco-2	colon:	n/a
40	chr7:118572128-118572178	CMK	blood:	n/a
41	chr7:118572128-118572178	U87	brain:	n/a
42	chr7:118572128-118572178	GM12891	blood:	n/a
43	chr7:118572128-118572178	BJ	skin:	n/a
44	chr7:118572128-118572178	NB4	blood:	n/a
45	chr7:118572128-118572178	HEEpiC	esophagus:	n/a
46	chr7:118572128-118572178	GM06990	blood:	n/a
47	chr7:118572128-118572178	SAEC	small airway:	n/a
48	chr7:118572128-118572178	GM19239	blood:	n/a
49	chr7:118572128-118572178	HCT-116	colon:	n/a
50	chr7:118572128-118572178	HEK293	kidney:	embryo

No.	Distal block	Cell Line	Cell type
1	chr7:118552988..118554537-chr7:118554629..118557088,2	MCF-7	breast:
2	chr7:118686305..118688542-chr7:118689075..118691425,2	MCF-7	breast:
3	chr7:118611978..118614798-chr7:118654699..118657373,2	K562	blood:
4	chr7:118541712..118543750-chr7:118545681..118548097,2	K562	blood:
5	chr7:118654140..118657090-chr7:118659038..118660634,2	K562	blood:
6	chr7:118654140..118657090-chr7:118659038..118660634,2	K562	blood:
7	chr7:118658923..118660731-chr7:118674082..118677043,2	K562	blood:
8	chr7:118637455..118640247-chr7:118654338..118656624,3	K562	blood:
9	chr7:118637455..118639784-chr7:118654717..118656624,2	K562	blood:
10	chr7:118733515..118736474-chr7:118742172..118744304,2	K562	blood:
11	chr7:118683308..118685172-chr7:118689159..118691068,2	K562	blood:
12	chr7:118629006..118631002-chr7:118732998..118734533,2	K562	blood:
13	chr7:118683308..118685172-chr7:118689159..118691068,2	K562	blood:
14	chr7:118558340..118559254-chr7:118837696..118838683,4	MCF-7	breast:
15	chr7:118637455..118640247-chr7:118654338..118656624,3	K562	blood:
16	chr7:118635764..118637617-chr7:118641365..118644121,2	MCF-7	breast:
17	chr7:118637455..118639784-chr7:118654717..118656624,2	K562	blood:
18	chr7:118629006..118631002-chr7:118732998..118734533,2	K562	blood:
19	chr7:118558904..118559746-chr7:118816086..118816731,2	MCF-7	breast:
20	chr7:118646033..118648474-chr7:118650936..118653090,2	K562	blood:
21	chr7:118611978..118614798-chr7:118654699..118657373,2	K562	blood:
22	chr7:118558392..118559287-chr7:118815693..118816489,5	MCF-7	breast:
23	chr7:118552988..118554537-chr7:118554629..118557088,2	MCF-7	breast:
24	chr7:118635764..118637617-chr7:118641365..118644121,2	MCF-7	breast:
25	chr7:118658923..118660731-chr7:118674082..118677043,2	K562	blood:
26	chr3:27629054..27629554-chr7:118565092..118565730,2	MCF-7	breast:
27	chr7:118541712..118543750-chr7:118545681..118548097,2	K562	blood:
28	chr7:118686305..118688542-chr7:118689075..118691425,2	MCF-7	breast:
29	chr7:118646033..118648474-chr7:118650936..118653090,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CTTNBP2-6	chr7:118590440-118591313	NONHSAT122979

Variant related genes	Relation type
ENSG00000230520	TF binding region
ENSG00000230520	CpG island

Extended variants
information (count: 2643 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:2643 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530800019	chr7:118543365-118543366	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs148020358	chr7:118543366-118543367	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs561398435	chr7:118543388-118543389	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs374147643	chr7:118543426-118543427	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs80297949	chr7:118543441-118543442	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs141726879	chr7:118543463-118543464	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs570590058	chr7:118543498-118543499	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs115742805	chr7:118543507-118543508	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs188463341	chr7:118543511-118543512	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs150131170	chr7:118543584-118543585	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs535810814	chr7:118543591-118543592	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs563466851	chr7:118545637-118545638	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs529150829	chr7:118545642-118545643	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs542849460	chr7:118545700-118545701	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs373503786	chr7:118545709-118545710	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs575645195	chr7:118545714-118545715	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs376118831	chr7:118545748-118545749	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs144722191	chr7:118545767-118545768	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs528402775	chr7:118545791-118545792	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs191383234	chr7:118545843-118545844	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs183066826	chr7:118545915-118545916	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs148543483	chr7:118545947-118545948	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs113725054	chr7:118546000-118546001	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs530897190	chr7:118546012-118546013	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs530565165	chr7:118546066-118546067	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs550701157	chr7:118546080-118546081	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs547754704	chr7:118546093-118546094	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs536401060	chr7:118546116-118546117	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs28676768	chr7:118546123-118546124	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs567016892	chr7:118546142-118546143	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs191019340	chr7:118546157-118546158	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs557443875	chr7:118546175-118546176	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs142880561	chr7:118546189-118546190	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs17141857	chr7:118546208-118546209	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs377195620	chr7:118546227-118546228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs573791968	chr7:118546229-118546230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs551983073	chr7:118546232-118546233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs73471513	chr7:118546277-118546278	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs570554122	chr7:118546395-118546396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs146599138	chr7:118546396-118546397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs565125154	chr7:118546444-118546445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs570667401	chr7:118546446-118546447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs546732741	chr7:118546454-118546455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs374626672	chr7:118546488-118546489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs140131355	chr7:118546507-118546508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs183498678	chr7:118546512-118546513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs550563196	chr7:118546516-118546517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs561005332	chr7:118546593-118546594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs187489751	chr7:118546664-118546665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs546848965	chr7:118546669-118546670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	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
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19401682	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Schizophrenia	21346763	CNVD
Myelofibrosis	22110671	CNVD
Renal cell carcinoma	18194544	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:104 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:118541400-118543600	Enhancers	HMEC	breast
2	chr7:118545600-118546000	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr7:118545600-118546200	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr7:118545800-118546200	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr7:118546200-118547200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr7:118547200-118547400	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr7:118548400-118548800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr7:118567800-118568800	Enhancers	Fetal Heart	heart
9	chr7:118571000-118572000	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr7:118571400-118571800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
11	chr7:118571400-118572200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr7:118571400-118573000	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr7:118571400-118573600	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr7:118571400-118573600	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr7:118571600-118573600	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr7:118572000-118572400	Active TSS	iPS-20b Cell Line	embryonic stem cell
17	chr7:118578800-118579000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
18	chr7:118579000-118579200	ZNF genes & repeats	Primary T helper memory cells from peripheral blood 1	blood
19	chr7:118579200-118581600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
20	chr7:118581600-118581800	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
21	chr7:118585800-118586400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr7:118585800-118586400	Enhancers	Cortex derived primary cultured neurospheres	brain
23	chr7:118586400-118589200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr7:118586800-118587000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr7:118596200-118597000	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr7:118597600-118597800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr7:118597600-118598600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr7:118598400-118598600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr7:118605600-118607000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr7:118607000-118608000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr7:118607600-118608000	Enhancers	Dnd41	blood
32	chr7:118608000-118608400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr7:118608400-118609600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr7:118609600-118609800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr7:118614400-118615200	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr7:118614600-118615000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr7:118614600-118615200	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr7:118614600-118615200	Enhancers	Fetal Brain Male	brain
39	chr7:118615000-118615400	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr7:118635000-118636200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr7:118635200-118635600	Enhancers	Fetal Lung	lung
42	chr7:118635600-118637000	Weak transcription	Fetal Lung	lung
43	chr7:118637000-118637600	Enhancers	Fetal Lung	lung
44	chr7:118637600-118639000	Weak transcription	Fetal Lung	lung
45	chr7:118639000-118639400	Flanking Active TSS	Fetal Lung	lung
46	chr7:118639400-118640200	Enhancers	Fetal Lung	lung
47	chr7:118639800-118640400	Enhancers	Fetal Brain Male	brain
48	chr7:118646600-118647800	Enhancers	Fetal Brain Male	brain
49	chr7:118646600-118648400	Enhancers	Fetal Lung	lung
50	chr7:118656800-118657800	Enhancers	HUES64 Cell Line	embryonic stem cell

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